ClinVar Miner

List of variants in gene MSH2 studied for Lynch syndrome I

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 301
Download table as spreadsheet
HGVS dbSNP
MSH2, DEL 50 CODONS
NM_000251.1(MSH2):c.-823_1076+5984del
NM_000251.2(MSH2):c.-179C>T rs17224094
NM_000251.2(MSH2):c.-181G>A rs786201698
NM_000251.2(MSH2):c.-182C>T rs876658327
NM_000251.2(MSH2):c.-225G>C rs138068023
NM_000251.2(MSH2):c.-3G>C rs587779960
NM_000251.2(MSH2):c.-81dupA rs587779187
NM_000251.2(MSH2):c.-9G>C rs547444746
NM_000251.2(MSH2):c.1006C>T (p.Pro336Ser) rs63751062
NM_000251.2(MSH2):c.1013G>C (p.Gly338Ala) rs587779065
NM_000251.2(MSH2):c.1015C>T (p.Gln339Ter) rs1558466577
NM_000251.2(MSH2):c.1021C>G (p.Leu341Val) rs748115066
NM_000251.2(MSH2):c.1030C>A (p.Gln344Lys) rs63750245
NM_000251.2(MSH2):c.1043A>G (p.Gln348Arg) rs773177076
NM_000251.2(MSH2):c.1046C>G (p.Pro349Arg) rs587779067
NM_000251.2(MSH2):c.1046_1047delinsGC (p.Pro349Arg) rs1558466685
NM_000251.2(MSH2):c.1070A>C (p.Glu357Ala) rs150503781
NM_000251.2(MSH2):c.1076+23C>G rs377417056
NM_000251.2(MSH2):c.1077-10T>C rs17224360
NM_000251.2(MSH2):c.1077-15G>T rs753277524
NM_000251.2(MSH2):c.1077-2A>C rs267607943
NM_000251.2(MSH2):c.108T>C (p.Leu36=) rs876659034
NM_000251.2(MSH2):c.1130A>G (p.Gln377Arg) rs776174711
NM_000251.2(MSH2):c.1144C>T (p.Arg382Cys) rs752373431
NM_000251.2(MSH2):c.1145G>A (p.Arg382His) rs267607947
NM_000251.2(MSH2):c.1147C>T (p.Arg383Ter) rs63749849
NM_000251.2(MSH2):c.114C>G (p.Asp38Glu) rs587779074
NM_000251.2(MSH2):c.115C>A (p.Arg39=) rs786202334
NM_000251.2(MSH2):c.1165C>T (p.Arg389Ter) rs587779075
NM_000251.2(MSH2):c.1171G>A (p.Ala391Thr) rs878853798
NM_000251.2(MSH2):c.1182T>G (p.Phe394Leu) rs374135434
NM_000251.2(MSH2):c.11A>T (p.Gln4Leu) rs754562075
NM_000251.2(MSH2):c.1203dup (p.Gln402fs) rs63750586
NM_000251.2(MSH2):c.1204C>A (p.Gln402Lys) rs63751412
NM_000251.2(MSH2):c.1216C>T (p.Arg406Ter) rs63751108
NM_000251.2(MSH2):c.1217G>A (p.Arg406Gln) rs146567853
NM_000251.2(MSH2):c.1223A>T (p.Tyr408Phe) rs63750379
NM_000251.2(MSH2):c.1226_1227del (p.Gln409fs) rs63750086
NM_000251.2(MSH2):c.123C>G (p.Asp41Glu) rs761960690
NM_000251.2(MSH2):c.1271A>G (p.His424Arg) rs200429136
NM_000251.2(MSH2):c.1271dup (p.His424fs) rs587783055
NM_000251.2(MSH2):c.1276+10G>A rs374061707
NM_000251.2(MSH2):c.1276+11A>G rs189015988
NM_000251.2(MSH2):c.1276+16G>A rs368120695
NM_000251.2(MSH2):c.1276+2T>C rs267607953
NM_000251.2(MSH2):c.1276+47T>A rs148018406
NM_000251.2(MSH2):c.1277-16T>C rs368653974
NM_000251.2(MSH2):c.1277-4076_1386+1819del
NM_000251.2(MSH2):c.1277-6224_1386+4836del
NM_000251.2(MSH2):c.1277-6284_1386+4776del
NM_000251.2(MSH2):c.128A>G (p.Tyr43Cys) rs17217723
NM_000251.2(MSH2):c.1311G>T (p.Val437=) rs730881781
NM_000251.2(MSH2):c.1313C>T (p.Thr438Ile) rs1553361185
NM_000251.2(MSH2):c.1313_1315CTC[1] (p.Pro439del) rs587779082
NM_000251.2(MSH2):c.1331G>T (p.Arg444Leu) rs557339938
NM_000251.2(MSH2):c.1344C>T (p.Ser448=) rs1010360604
NM_000251.2(MSH2):c.1347G>C (p.Lys449Asn) rs587781331
NM_000251.2(MSH2):c.1382A>C (p.Asp461Ala) rs730881756
NM_000251.2(MSH2):c.1387-8G>T rs187525243
NM_000251.2(MSH2):c.1387-9T>A rs587779087
NM_000251.2(MSH2):c.1387-9T>C rs587779087
NM_000251.2(MSH2):c.142G>T (p.Glu48Ter) rs63750615
NM_000251.2(MSH2):c.1453_1456ATGA[1] (p.Asn486fs) rs1114167806
NM_000251.2(MSH2):c.1461C>G (p.Asp487Glu) rs35107951
NM_000251.2(MSH2):c.1462T>G (p.Leu488Val) rs587781314
NM_000251.2(MSH2):c.1465G>A (p.Glu489Lys) rs876658187
NM_000251.2(MSH2):c.146A>T (p.Asp49Val) rs63750335
NM_000251.2(MSH2):c.1488A>G (p.Leu496=) rs267607960
NM_000251.2(MSH2):c.149C>G (p.Ala50Gly) rs876658582
NM_000251.2(MSH2):c.14C>A (p.Pro5Gln) rs56170584
NM_000251.2(MSH2):c.1510+11G>C rs370675562
NM_000251.2(MSH2):c.1510G>C (p.Gly504Arg) rs63751600
NM_000251.2(MSH2):c.1511-41G>C rs202215396
NM_000251.2(MSH2):c.1511-9A>T rs12998837
NM_000251.2(MSH2):c.1547G>T (p.Ser516Ile) rs373564353
NM_000251.2(MSH2):c.1560A>G (p.Gly520=) rs63750820
NM_000251.2(MSH2):c.1563T>C (p.Tyr521=) rs63750330
NM_000251.2(MSH2):c.1571G>C (p.Arg524Pro) rs63751207
NM_000251.2(MSH2):c.1571G>T (p.Arg524Leu) rs63751207
NM_000251.2(MSH2):c.1582A>C (p.Lys528Gln) rs199744440
NM_000251.2(MSH2):c.1600C>T (p.Arg534Cys) rs63750029
NM_000251.2(MSH2):c.1601G>A (p.Arg534His) rs587778523
NM_000251.2(MSH2):c.1601G>T (p.Arg534Leu) rs587778523
NM_000251.2(MSH2):c.160G>T (p.Ala54Ser) rs749212640
NM_000251.2(MSH2):c.163C>T (p.Arg55Trp)
NM_000251.2(MSH2):c.1640A>G (p.Asn547Ser) rs267607967
NM_000251.2(MSH2):c.1661+12G>A rs3732183
NM_000251.2(MSH2):c.1661+17T>G rs377461923
NM_000251.2(MSH2):c.1661+25delT rs1553366691
NM_000251.2(MSH2):c.1662-18T>C rs376235435
NM_000251.2(MSH2):c.1662-23A>G rs56404027
NM_000251.2(MSH2):c.1662-9G>A rs17218356
NM_000251.2(MSH2):c.1666T>C (p.Leu556=) rs61756466
NM_000251.2(MSH2):c.1667T>G (p.Leu556Trp) rs587779101
NM_000251.2(MSH2):c.1681G>A (p.Glu561Lys) rs63750328
NM_000251.2(MSH2):c.1690A>G (p.Thr564Ala) rs55778204
NM_000251.2(MSH2):c.1692_1693del (p.Lys565_Asn566insTer) rs1553367635
NM_000251.2(MSH2):c.1705_1706del (p.Glu569fs) rs63750393
NM_000251.2(MSH2):c.1706A>G (p.Glu569Gly) rs786201077
NM_000251.2(MSH2):c.1708del (p.Tyr570fs) rs1131692279
NM_000251.2(MSH2):c.1730T>C (p.Ile577Thr) rs63749910
NM_000251.2(MSH2):c.1737A>G (p.Lys579=) rs61756467
NM_000251.2(MSH2):c.1748A>T (p.Asn583Ile) rs201118107
NM_000251.2(MSH2):c.1759+16C>G rs1057517573
NM_000251.2(MSH2):c.1760-10T>A rs767536391
NM_000251.2(MSH2):c.1760-16T>G rs768370188
NM_000251.2(MSH2):c.1774A>G (p.Met592Val) rs371614039
NM_000251.2(MSH2):c.1786_1788del (p.Asn596del) rs63749831
NM_000251.2(MSH2):c.1787A>G (p.Asn596Ser) rs41295288
NM_000251.2(MSH2):c.1790A>C (p.Asp597Ala) rs548407418
NM_000251.2(MSH2):c.1796T>C (p.Leu599Ser) rs747504492
NM_000251.2(MSH2):c.1804C>G (p.Leu602Val) rs748797209
NM_000251.2(MSH2):c.1813G>T (p.Val605Phe) rs730881777
NM_000251.2(MSH2):c.1817T>C (p.Val606Ala) rs376044376
NM_000251.2(MSH2):c.1828C>A (p.His610Asn) rs267607980
NM_000251.2(MSH2):c.182A>C (p.Gln61Pro) rs587779113
NM_000251.2(MSH2):c.1831G>A (p.Val611Met) rs369385048
NM_000251.2(MSH2):c.1847C>G (p.Pro616Arg) rs587779965
NM_000251.2(MSH2):c.1854A>G (p.Pro618=) rs786203744
NM_000251.2(MSH2):c.1861C>T (p.Arg621Ter) rs63750508
NM_000251.2(MSH2):c.1862G>A (p.Arg621Gln) rs759263820
NM_000251.2(MSH2):c.1865C>A (p.Pro622Gln) rs28929483
NM_000251.2(MSH2):c.1865C>T (p.Pro622Leu) rs28929483
NM_000251.2(MSH2):c.1884A>T (p.Gly628=) rs786202663
NM_000251.2(MSH2):c.1886A>G (p.Gln629Arg) rs61756468
NM_000251.2(MSH2):c.1897A>G (p.Ile633Val) rs771695599
NM_000251.2(MSH2):c.1906G>C (p.Ala636Pro) rs63750875
NM_000251.2(MSH2):c.1915C>T (p.His639Tyr) rs28929484
NM_000251.2(MSH2):c.1933C>G (p.Gln645Glu) rs267607982
NM_000251.2(MSH2):c.1963G>A (p.Val655Ile) rs549467183
NM_000251.2(MSH2):c.1979A>G (p.Asp660Gly) rs1085308057
NM_000251.2(MSH2):c.1986G>C (p.Gln662His) rs587780685
NM_000251.2(MSH2):c.198C>T (p.Tyr66=) rs730881784
NM_000251.2(MSH2):c.1A>C (p.Met1Leu) rs267607911
NM_000251.2(MSH2):c.1A>G (p.Met1Val) rs267607911
NM_000251.2(MSH2):c.2005+8dup rs267607992
NM_000251.2(MSH2):c.2005G>C (p.Gly669Arg) rs63751668
NM_000251.2(MSH2):c.2006-26dup rs781614743
NM_000251.2(MSH2):c.2006-4G>A rs369853630
NM_000251.2(MSH2):c.2006-6T>C rs2303428
NM_000251.2(MSH2):c.200T>A (p.Met67Lys) rs876660001
NM_000251.2(MSH2):c.2038C>T (p.Arg680Ter) rs63749932
NM_000251.2(MSH2):c.2048G>T (p.Gly683Val) rs755920849
NM_000251.2(MSH2):c.2061C>G (p.Leu687=) rs63750032
NM_000251.2(MSH2):c.2064G>A (p.Met688Ile) rs63750790
NM_000251.2(MSH2):c.2074G>T (p.Gly692Trp) rs63750232
NM_000251.2(MSH2):c.2075G>T (p.Gly692Val) rs63751432
NM_000251.2(MSH2):c.2090G>A (p.Cys697Tyr) rs63750398
NM_000251.2(MSH2):c.211+8C>T rs267607916
NM_000251.2(MSH2):c.211+9C>G rs2303426
NM_000251.2(MSH2):c.2111T>C (p.Ile704Thr) rs564657106
NM_000251.2(MSH2):c.2113del (p.Val705fs) rs63749811
NM_000251.2(MSH2):c.212-4delT rs746333570
NM_000251.2(MSH2):c.2120G>A (p.Cys707Tyr) rs373226409
NM_000251.2(MSH2):c.2139G>T (p.Gly713=) rs63750003
NM_000251.2(MSH2):c.213A>G (p.Gly71=) rs878853808
NM_000251.2(MSH2):c.2164G>T (p.Val722Phe) rs587781996
NM_000251.2(MSH2):c.2197G>A (p.Ala733Thr) rs772662439
NM_000251.2(MSH2):c.2203A>G (p.Ile735Val) rs2229061
NM_000251.2(MSH2):c.2205C>T (p.Ile735=) rs533553381
NM_000251.2(MSH2):c.220A>C (p.Asn74His) rs150548839
NM_000251.2(MSH2):c.2210+11_2210+22del rs730881782
NM_000251.2(MSH2):c.2211-5T>G rs368596736
NM_000251.2(MSH2):c.2211-6C>A rs267608003
NM_000251.2(MSH2):c.2251G>C (p.Gly751Arg) rs63751119
NM_000251.2(MSH2):c.2293G>A (p.Ala765Thr) rs63750368
NM_000251.2(MSH2):c.2304del (p.Glu768fs) rs587783053
NM_000251.2(MSH2):c.2308A>G (p.Ile770Val) rs63750684
NM_000251.2(MSH2):c.2334C>A (p.Cys778Ter) rs63750618
NM_000251.2(MSH2):c.2363_2364del (p.Thr788fs) rs63750937
NM_000251.2(MSH2):c.2375A>G (p.Asn792Ser) rs587782891
NM_000251.2(MSH2):c.23C>T (p.Thr8Met) rs17217716
NM_000251.2(MSH2):c.2400A>G (p.Leu800=) rs201298777
NM_000251.2(MSH2):c.2437A>G (p.Met813Val) rs63749841
NM_000251.2(MSH2):c.2458+12T>C rs1553369841
NM_000251.2(MSH2):c.2458+16G>A rs373624698
NM_000251.2(MSH2):c.2458+8C>G rs189025757
NM_000251.2(MSH2):c.2459G>A (p.Gly820Asp) rs794729229
NM_000251.2(MSH2):c.2500G>A (p.Ala834Thr) rs63750757
NM_000251.2(MSH2):c.2503A>C (p.Asn835His) rs41295296
NM_000251.2(MSH2):c.2523_2524AG[1] (p.Glu842fs) rs587779148
NM_000251.2(MSH2):c.2525A>T (p.Glu842Val) rs373393954
NM_000251.2(MSH2):c.2533A>G (p.Lys845Glu) rs63750571
NM_000251.2(MSH2):c.2537A>G (p.Gln846Arg) rs140754514
NM_000251.2(MSH2):c.2551C>A (p.Leu851Ile) rs267608015
NM_000251.2(MSH2):c.2556G>C (p.Glu852Asp) rs587781453
NM_000251.2(MSH2):c.2558A>C (p.Glu853Ala) rs63750797
NM_000251.2(MSH2):c.2567A>G (p.Tyr856Cys) rs587779150
NM_000251.2(MSH2):c.2576_2584del (p.Glu859_Gln861del) rs587781278
NM_000251.2(MSH2):c.2579C>A (p.Ser860Ter) rs63750849
NM_000251.2(MSH2):c.260C>G (p.Ser87Cys) rs587781447
NM_000251.2(MSH2):c.2615A>G (p.Lys872Arg) rs587780686
NM_000251.2(MSH2):c.2629_2630AG[2] (p.Glu878fs) rs63751618
NM_000251.2(MSH2):c.2634+12T>C rs372907481
NM_000251.2(MSH2):c.2635-2A>G
NM_000251.2(MSH2):c.2635C>T (p.Gln879Ter) rs63751469
NM_000251.2(MSH2):c.2647del (p.Ile883fs) rs63750084
NM_000251.2(MSH2):c.2647dup (p.Ile883fs) rs63750084
NM_000251.2(MSH2):c.2653C>T (p.Gln885Ter) rs63750808
NM_000251.2(MSH2):c.2662del (p.Leu888fs) rs63751007
NM_000251.2(MSH2):c.2714C>G (p.Thr905Arg) rs267608022
NM_000251.2(MSH2):c.2717T>C (p.Ile906Thr) rs587780687
NM_000251.2(MSH2):c.2722T>A (p.Leu908Ile) rs1085308059
NM_000251.2(MSH2):c.2726A>T (p.Lys909Ile) rs34319539
NM_000251.2(MSH2):c.2732T>G (p.Leu911Arg) rs41295182
NM_000251.2(MSH2):c.2740G>T (p.Glu914Ter) rs267608024
NM_000251.2(MSH2):c.274C>G (p.Leu92Val) rs587779154
NM_000251.2(MSH2):c.2766T>C (p.Phe922=) rs55859129
NM_000251.2(MSH2):c.2777T>A (p.Ile926Asn) rs199747712
NM_000251.2(MSH2):c.2785C>T (p.Arg929Ter) rs551060742
NM_000251.2(MSH2):c.2786G>A (p.Arg929Gln) rs587779967
NM_000251.2(MSH2):c.2789T>A (p.Ile930Lys) rs587783054
NM_000251.2(MSH2):c.2790A>G (p.Ile930Met) rs587779155
NM_000251.2(MSH2):c.2801C>A (p.Thr934Lys) rs587779969
NM_000251.2(MSH2):c.2802G>A (p.Thr934=) rs150259097
NM_000251.2(MSH2):c.287G>A (p.Arg96His) rs63750002
NM_000251.2(MSH2):c.289C>T (p.Gln97Ter) rs63750970
NM_000251.2(MSH2):c.301_306del (p.Glu101_Val102del) rs587779157
NM_000251.2(MSH2):c.304G>A (p.Val102Ile) rs193922373
NM_000251.2(MSH2):c.308A>G (p.Tyr103Cys) rs63751173
NM_000251.2(MSH2):c.317G>A (p.Arg106Lys) rs41295286
NM_000251.2(MSH2):c.336C>A (p.Ser112=) rs34312619
NM_000251.2(MSH2):c.339G>A (p.Lys113=) rs35898375
NM_000251.2(MSH2):c.354T>G (p.Tyr118Ter) rs1553350250
NM_000251.2(MSH2):c.366+24A>G rs200890440
NM_000251.2(MSH2):c.366+25C>T rs764158568
NM_000251.2(MSH2):c.367-19A>T rs730881783
NM_000251.2(MSH2):c.376G>C (p.Gly126Arg) rs767371843
NM_000251.2(MSH2):c.380A>G (p.Asn127Ser) rs17217772
NM_000251.2(MSH2):c.383T>G (p.Leu128Arg) rs730881768
NM_000251.2(MSH2):c.399C>T (p.Asp133=) rs61756462
NM_000251.2(MSH2):c.403C>T (p.Leu135Phe) rs193096019
NM_000251.2(MSH2):c.42G>A (p.Ala14=) rs374396150
NM_000251.2(MSH2):c.433A>G (p.Ile145Val) rs876659264
NM_000251.2(MSH2):c.435T>G (p.Ile145Met) rs63750124
NM_000251.2(MSH2):c.437G>T (p.Gly146Val) rs772052262
NM_000251.2(MSH2):c.438T>C (p.Gly146=) rs587779161
NM_000251.2(MSH2):c.459C>T (p.Ser153=) rs63751065
NM_000251.2(MSH2):c.464T>A (p.Val155Asp) rs876658188
NM_000251.2(MSH2):c.470G>C (p.Gly157Ala) rs765489269
NM_000251.2(MSH2):c.471C>A (p.Gly157=) rs61756463
NM_000251.2(MSH2):c.482T>A (p.Val161Asp) rs63750126
NM_000251.2(MSH2):c.484G>A (p.Gly162Arg) rs63750624
NM_000251.2(MSH2):c.488T>G (p.Val163Gly) rs63750214
NM_000251.2(MSH2):c.499G>C (p.Asp167His) rs63750255
NM_000251.2(MSH2):c.4G>A (p.Ala2Thr) rs63750466
NM_000251.2(MSH2):c.505A>G (p.Ile169Val) rs63750716
NM_000251.2(MSH2):c.507A>G (p.Ile169Met) rs748762580
NM_000251.2(MSH2):c.518T>G (p.Leu173Arg) rs63750070
NM_000251.2(MSH2):c.557A>G (p.Asn186Ser) rs151129360
NM_000251.2(MSH2):c.55T>C (p.Phe19Leu) rs141711342
NM_000251.2(MSH2):c.566C>G (p.Ala189Gly) rs141021599
NM_000251.2(MSH2):c.573C>T (p.Leu191=) rs1800151
NM_000251.2(MSH2):c.599T>A (p.Val200Asp) rs587779167
NM_000251.2(MSH2):c.5C>T (p.Ala2Val) rs587778521
NM_000251.2(MSH2):c.606C>T (p.Pro202=) rs63750600
NM_000251.2(MSH2):c.607G>A (p.Gly203Arg) rs587779973
NM_000251.2(MSH2):c.610G>A (p.Gly204Arg) rs63750574
NM_000251.2(MSH2):c.646-3T>C rs267607930
NM_000251.2(MSH2):c.672C>G (p.Ile224Met) rs587779171
NM_000251.2(MSH2):c.6G>T (p.Ala2=) rs368270856
NM_000251.2(MSH2):c.701C>T (p.Thr234Ile) rs730881773
NM_000251.2(MSH2):c.715C>T (p.Gln239Ter) rs63750488
NM_000251.2(MSH2):c.716A>G (p.Gln239Arg) rs199676483
NM_000251.2(MSH2):c.728G>A (p.Arg243Gln) rs63751455
NM_000251.2(MSH2):c.762T>C (p.Asn254=) rs587779180
NM_000251.2(MSH2):c.766G>A (p.Ala256Thr) rs377403073
NM_000251.2(MSH2):c.792+5A>G rs267607935
NM_000251.2(MSH2):c.792G>C (p.Gln264His) rs587779183
NM_000251.2(MSH2):c.806C>A (p.Ser269Ter) rs63750058
NM_000251.2(MSH2):c.80C>T (p.Pro27Leu) rs750746034
NM_000251.2(MSH2):c.811_814del (p.Ser271fs) rs587779185
NM_000251.2(MSH2):c.815C>T (p.Ala272Val) rs34136999
NM_000251.2(MSH2):c.820A>G (p.Ile274Val) rs371944271
NM_000251.2(MSH2):c.835C>G (p.Leu279Val) rs375351205
NM_000251.2(MSH2):c.845A>G (p.Asp282Gly) rs587779978
NM_000251.2(MSH2):c.860_868del (p.Gly287_Phe289del) rs864622042
NM_000251.2(MSH2):c.885C>G (p.Asp295Glu) rs201334592
NM_000251.2(MSH2):c.888C>G (p.Phe296Leu) rs876659918
NM_000251.2(MSH2):c.89C>T (p.Pro30Leu) rs757892928
NM_000251.2(MSH2):c.905T>A (p.Leu302Ter) rs63749914
NM_000251.2(MSH2):c.934C>G (p.Leu312Val) rs756398636
NM_000251.2(MSH2):c.942+1delG rs1194793421
NM_000251.2(MSH2):c.942+28_942+29del rs11309117
NM_000251.2(MSH2):c.942+3A>T rs193922376
NM_000251.2(MSH2):c.942+3delA rs11309117
NM_000251.2(MSH2):c.943-25T>C rs775155213
NM_000251.2(MSH2):c.943-2A>G rs587779198
NM_000251.2(MSH2):c.965G>A (p.Gly322Asp) rs4987188
NM_000251.2(MSH2):c.965G>T (p.Gly322Val) rs4987188
NM_000251.2(MSH2):c.968C>G (p.Ser323Cys) rs63750732
NM_000251.2(MSH2):c.968C>T (p.Ser323Phe) rs63750732
NM_000251.2(MSH2):c.972G>A (p.Gln324=) rs63750505
NM_000251.2(MSH2):c.97A>C (p.Thr33Pro) rs63751107
NM_000251.2(MSH2):c.982G>A (p.Ala328Thr) rs753237286
NM_000251.2(MSH2):c.982G>C (p.Ala328Pro) rs753237286
NM_000251.2(MSH2):c.984C>T (p.Ala328=) rs4987189
NM_000251.2(MSH2):c.991A>G (p.Asn331Asp) rs267607938
NM_000251.2(MSH2):c.998G>A (p.Cys333Tyr) rs63750828
nsv513794

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.