ClinVar Miner

List of variants in gene LAMA2 reported by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 242
Download table as spreadsheet
HGVS dbSNP
NM_000426.3(LAMA2):c.-17delC rs537351244
NM_000426.3(LAMA2):c.113-14T>A rs1311979480
NM_000426.3(LAMA2):c.1206+11C>T rs115007959
NM_000426.3(LAMA2):c.1279_1280delGT (p.Val427Glnfs) rs1554230429
NM_000426.3(LAMA2):c.12delC (p.Ala5Profs) rs1554312639
NM_000426.3(LAMA2):c.1303C>T (p.Arg435Ter) rs773209126
NM_000426.3(LAMA2):c.1308T>G (p.Gly436=) rs41285286
NM_000426.3(LAMA2):c.1373G>A (p.Arg458Lys) rs140604077
NM_000426.3(LAMA2):c.1403C>G (p.Ala468Gly) rs111695726
NM_000426.3(LAMA2):c.1468-19T>C rs200241408
NM_000426.3(LAMA2):c.1491T>C (p.Cys497=) rs2306220
NM_000426.3(LAMA2):c.1499G>A (p.Cys500Tyr) rs1064794941
NM_000426.3(LAMA2):c.1533T>C (p.Asn511=) rs9492266
NM_000426.3(LAMA2):c.1558T>A (p.Cys520Ser) rs886061046
NM_000426.3(LAMA2):c.156C>T (p.Ile52=) rs1140366
NM_000426.3(LAMA2):c.1586G>A (p.Ser529Asn) rs370691060
NM_000426.3(LAMA2):c.1609-41_1609-7=
NM_000426.3(LAMA2):c.1621A>G (p.Ser541Gly) rs141363186
NM_000426.3(LAMA2):c.1634T>A (p.Leu545Gln) rs118083923
NM_000426.3(LAMA2):c.1657C>T (p.Arg553Ter) rs1303773212
NM_000426.3(LAMA2):c.1670A>C (p.Gln557Pro) rs1333451961
NM_000426.3(LAMA2):c.1701C>T (p.Ile567=) rs111381107
NM_000426.3(LAMA2):c.1762delG (p.Ala588Leufs) rs786205654
NM_000426.3(LAMA2):c.1781_1782delAA (p.Lys594Thrfs) rs1554238384
NM_000426.3(LAMA2):c.1782+14T>C rs191215452
NM_000426.3(LAMA2):c.1792G>A (p.Val598Ile) rs753232836
NM_000426.3(LAMA2):c.1814C>T (p.Thr605Ile) rs112388307
NM_000426.3(LAMA2):c.1816A>G (p.Ile606Val) rs113022759
NM_000426.3(LAMA2):c.1854_1861dupACGTGTTC (p.Leu621Hisfs) rs202247791
NM_000426.3(LAMA2):c.1856G>A (p.Arg619His) rs3816665
NM_000426.3(LAMA2):c.1885-19C>A rs372219177
NM_000426.3(LAMA2):c.1930C>G (p.His644Asp) rs35879899
NM_000426.3(LAMA2):c.2049_2050delAG rs202247790
NM_000426.3(LAMA2):c.2054T>C (p.Leu685Pro) rs746641607
NM_000426.3(LAMA2):c.2084A>T (p.Asp695Val) rs762272518
NM_000426.3(LAMA2):c.2097-13T>C rs139246515
NM_000426.3(LAMA2):c.2115T>G (p.Leu705=) rs149753273
NM_000426.3(LAMA2):c.2187G>C (p.Gly729=) rs142345851
NM_000426.3(LAMA2):c.2265G>A (p.Glu755=) rs910253334
NM_000426.3(LAMA2):c.2288C>T (p.Ala763Val) rs141521127
NM_000426.3(LAMA2):c.2304C>T (p.Asp768=) rs142126511
NM_000426.3(LAMA2):c.2323-18T>A rs199846930
NM_000426.3(LAMA2):c.2323-19A>T rs139093294
NM_000426.3(LAMA2):c.2350dupT (p.Tyr784Leufs) rs1554260284
NM_000426.3(LAMA2):c.2382C>T (p.Gly794=) rs147744763
NM_000426.3(LAMA2):c.2430A>C (p.Pro810=) rs147572139
NM_000426.3(LAMA2):c.2430A>G (p.Pro810=) rs147572139
NM_000426.3(LAMA2):c.2450+16A>G rs1024374408
NM_000426.3(LAMA2):c.2451-18G>A rs142989915
NM_000426.3(LAMA2):c.2462C>T (p.Thr821Met) rs117422805
NM_000426.3(LAMA2):c.2476C>T (p.Arg826Trp) rs118147866
NM_000426.3(LAMA2):c.2537+12C>T rs376097319
NM_000426.3(LAMA2):c.255C>T (p.Ile85=) rs142083777
NM_000426.3(LAMA2):c.2564C>G (p.Pro855Arg) rs754714449
NM_000426.3(LAMA2):c.2756G>T (p.Arg919Leu) rs35277491
NM_000426.3(LAMA2):c.2766C>T (p.Ala922=) rs149254699
NM_000426.3(LAMA2):c.2767G>A (p.Gly923Ser) rs144492513
NM_000426.3(LAMA2):c.2780C>T (p.Ser927Phe) rs1085307732
NM_000426.3(LAMA2):c.2799A>G (p.Gln933=) rs1027199
NM_000426.3(LAMA2):c.283+1G>A rs200288072
NM_000426.3(LAMA2):c.2856+13G>A rs149487202
NM_000426.3(LAMA2):c.2857-13C>T rs201188972
NM_000426.3(LAMA2):c.2932G>A (p.Asp978Asn) rs202050052
NM_000426.3(LAMA2):c.3154A>G (p.Ser1052Gly) rs149165006
NM_000426.3(LAMA2):c.3175-19G>C rs184243762
NM_000426.3(LAMA2):c.3215delG (p.Cys1072Serfs) rs886041297
NM_000426.3(LAMA2):c.3244C>T (p.His1082Tyr) rs146490004
NM_000426.3(LAMA2):c.3411+13G>A rs3798663
NM_000426.3(LAMA2):c.3412G>A (p.Val1138Met) rs2306942
NM_000426.3(LAMA2):c.3429C>A (p.Ile1143=) rs200646230
NM_000426.3(LAMA2):c.3461G>T (p.Gly1154Val) rs922954882
NM_000426.3(LAMA2):c.3532G>A (p.Ala1178Thr) rs34505698
NM_000426.3(LAMA2):c.3555+1G>A rs1057518119
NM_000426.3(LAMA2):c.3556-15T>G rs17741922
NM_000426.3(LAMA2):c.3582T>C (p.Ile1194=) rs137962409
NM_000426.3(LAMA2):c.3597T>C (p.Asp1199=) rs199904029
NM_000426.3(LAMA2):c.3613A>G (p.Thr1205Ala) rs35889149
NM_000426.3(LAMA2):c.3615G>A (p.Thr1205=) rs374656305
NM_000426.3(LAMA2):c.3630delT (p.Ile1210Metfs) rs398123372
NM_000426.3(LAMA2):c.3636delT (p.Gln1213Asnfs) rs1064795451
NM_000426.3(LAMA2):c.3799_3821del23 (p.Phe1267Aspfs) rs750220830
NM_000426.3(LAMA2):c.381C>A (p.Thr127=) rs4404787
NM_000426.3(LAMA2):c.3850G>C (p.Ala1284Pro) rs1085307846
NM_000426.3(LAMA2):c.397-15G>A rs188045427
NM_000426.3(LAMA2):c.397-15_397-13delGTT rs748624866
NM_000426.3(LAMA2):c.397-35_397del36 rs1554217476
NM_000426.3(LAMA2):c.3976C>T (p.Arg1326Ter) rs398123373
NM_000426.3(LAMA2):c.4002T>G (p.Tyr1334Ter)
NM_000426.3(LAMA2):c.4059-20T>C rs764866830
NM_000426.3(LAMA2):c.4060A>G (p.Ile1354Val) rs143674727
NM_000426.3(LAMA2):c.408C>T (p.Ile136=) rs145149634
NM_000426.3(LAMA2):c.411G>A (p.Ala137=) rs149347601
NM_000426.3(LAMA2):c.4176+9C>T rs117116822
NM_000426.3(LAMA2):c.4296A>G (p.Glu1432=) rs1423553661
NM_000426.3(LAMA2):c.4349G>A (p.Arg1450Gln) rs148905630
NM_000426.3(LAMA2):c.437C>T (p.Ser146Phe) rs143680577
NM_000426.3(LAMA2):c.4436+5G>T rs1057524616
NM_000426.3(LAMA2):c.4436+6A>G rs1057523624
NM_000426.3(LAMA2):c.4437-5T>A rs41285288
NM_000426.3(LAMA2):c.4470C>T (p.Asp1490=) rs35089085
NM_000426.3(LAMA2):c.4471G>A (p.Asp1491Asn) rs375640462
NM_000426.3(LAMA2):c.4487C>T (p.Ala1496Val) rs147077184
NM_000426.3(LAMA2):c.4523+19C>T rs17057158
NM_000426.3(LAMA2):c.4523G>A (p.Arg1508Lys) rs770084568
NM_000426.3(LAMA2):c.4646G>A (p.Arg1549Gln) rs778508100
NM_000426.3(LAMA2):c.4656C>A (p.Ala1552=) rs1057524318
NM_000426.3(LAMA2):c.4657A>G (p.Thr1553Ala) rs1450772080
NM_000426.3(LAMA2):c.4682delA (p.Lys1561Serfs) rs1246940477
NM_000426.3(LAMA2):c.4717+12_4717+20dupAACTTTGCT rs761353189
NM_000426.3(LAMA2):c.4717+1G>T rs1131691660
NM_000426.3(LAMA2):c.4740C>A (p.Gly1580=) rs371629354
NM_000426.3(LAMA2):c.4750G>A (p.Gly1584Ser) rs117781224
NM_000426.3(LAMA2):c.479A>G (p.Asp160Gly) rs147398243
NM_000426.3(LAMA2):c.4857A>G (p.Leu1619=) rs777158791
NM_000426.3(LAMA2):c.4926A>G (p.Thr1642=) rs62421010
NM_000426.3(LAMA2):c.4935C>A (p.Thr1645=) rs35579821
NM_000426.3(LAMA2):c.4956C>G (p.Thr1652=) rs17057184
NM_000426.3(LAMA2):c.4959+6G>T rs148060790
NM_000426.3(LAMA2):c.4960-16G>A rs9483026
NM_000426.3(LAMA2):c.4960-17C>A rs758048596
NM_000426.3(LAMA2):c.498G>A (p.Trp166Ter) rs553221833
NM_000426.3(LAMA2):c.5071+18A>G rs73591259
NM_000426.3(LAMA2):c.518A>T (p.Asp173Val) rs767671585
NM_000426.3(LAMA2):c.5234+19A>G rs1554287019
NM_000426.3(LAMA2):c.5235-8G>A rs1554287355
NM_000426.3(LAMA2):c.5247C>T (p.Ala1749=) rs149951387
NM_000426.3(LAMA2):c.525G>C (p.Glu175Asp) rs1554217596
NM_000426.3(LAMA2):c.5260delG (p.Val1754Terfs) rs794727594
NM_000426.3(LAMA2):c.5291A>G (p.Glu1764Gly) rs141950826
NM_000426.3(LAMA2):c.5317C>T (p.Arg1773Trp) rs138695453
NM_000426.3(LAMA2):c.5374G>T (p.Glu1792Ter) rs746201268
NM_000426.3(LAMA2):c.5448A>G (p.Lys1816=) rs1554289590
NM_000426.3(LAMA2):c.5454G>A (p.Lys1818=) rs759312395
NM_000426.3(LAMA2):c.5466A>G (p.Glu1822=) rs3749877
NM_000426.3(LAMA2):c.5469C>T (p.Ser1823=) rs753886576
NM_000426.3(LAMA2):c.5476C>T (p.Arg1826Ter) rs747349942
NM_000426.3(LAMA2):c.5502G>A (p.Glu1834=) rs3749878
NM_000426.3(LAMA2):c.5530C>A (p.Arg1844Ser) rs56173620
NM_000426.3(LAMA2):c.5530C>T (p.Arg1844Cys) rs56173620
NM_000426.3(LAMA2):c.5598G>T (p.Met1866Ile) rs1554289926
NM_000426.3(LAMA2):c.5633C>T (p.Ser1878Phe) rs139586720
NM_000426.3(LAMA2):c.5688C>T (p.His1896=) rs573779258
NM_000426.3(LAMA2):c.5833G>A (p.Ala1945Thr) rs3828736
NM_000426.3(LAMA2):c.5866-15T>C rs774886204
NM_000426.3(LAMA2):c.5866-1G>A rs1064797040
NM_000426.3(LAMA2):c.5969-4G>A rs566302197
NM_000426.3(LAMA2):c.5969-6T>C rs201913996
NM_000426.3(LAMA2):c.5978A>G (p.Asp1993Gly) rs752249871
NM_000426.3(LAMA2):c.6002G>A (p.Arg2001Lys) rs151009169
NM_000426.3(LAMA2):c.6047T>C (p.Leu2016Ser) rs773309064
NM_000426.3(LAMA2):c.6062dup (p.Leu2023Valfs) rs1554297242
NM_000426.3(LAMA2):c.6085+17C>T rs185719358
NM_000426.3(LAMA2):c.6128A>G (p.Gln2043Arg) rs144155507
NM_000426.3(LAMA2):c.6150T>C (p.Asp2050=) rs114766691
NM_000426.3(LAMA2):c.6167C>A (p.Thr2056Lys) rs73775407
NM_000426.3(LAMA2):c.61_62delCA (p.Gln21Glyfs) rs1554312687
NM_000426.3(LAMA2):c.6234A>G (p.Lys2078=) rs56920166
NM_000426.3(LAMA2):c.6237G>A (p.Thr2079=) rs2297738
NM_000426.3(LAMA2):c.6274+4C>T rs73775410
NM_000426.3(LAMA2):c.6274+5G>T rs367765202
NM_000426.3(LAMA2):c.6279C>T (p.Ala2093=) rs141190803
NM_000426.3(LAMA2):c.6339C>T (p.Leu2113=) rs752356162
NM_000426.3(LAMA2):c.6345C>T (p.Pro2115=) rs200364660
NM_000426.3(LAMA2):c.6430-18A>G rs1424400019
NM_000426.3(LAMA2):c.6430-5dupT rs550488535
NM_000426.3(LAMA2):c.6488delA (p.Lys2163Argfs) rs886039482
NM_000426.3(LAMA2):c.6539A>T (p.Asp2180Val) rs567385461
NM_000426.3(LAMA2):c.6605G>T (p.Gly2202Val) rs1554299897
NM_000426.3(LAMA2):c.6649G>A (p.Val2217Ile) rs147857398
NM_000426.3(LAMA2):c.665G>C (p.Arg222Thr) rs1267371641
NM_000426.3(LAMA2):c.6666G>A (p.Leu2222=) rs772358536
NM_000426.3(LAMA2):c.6697G>A (p.Val2233Ile) rs150945378
NM_000426.3(LAMA2):c.6708-3A>C rs112637707
NM_000426.3(LAMA2):c.670A>G (p.Ser224Gly) rs1085307718
NM_000426.3(LAMA2):c.675C>T (p.Ala225=) rs139665175
NM_000426.3(LAMA2):c.6788C>T (p.Thr2263Met) rs56209257
NM_000426.3(LAMA2):c.6832A>G (p.Met2278Val) rs146854942
NM_000426.3(LAMA2):c.6955C>T (p.Arg2319Ter) rs398123383
NM_000426.3(LAMA2):c.6992+5G>A rs1221715098
NM_000426.3(LAMA2):c.7058G>A (p.Arg2353His) rs548483084
NM_000426.3(LAMA2):c.7074C>A (p.Tyr2358Ter) rs762806915
NM_000426.3(LAMA2):c.7111T>G (p.Phe2371Val) rs150644209
NM_000426.3(LAMA2):c.7112T>G (p.Phe2371Cys) rs201274841
NM_000426.3(LAMA2):c.711C>T (p.Ser237=) rs369745832
NM_000426.3(LAMA2):c.7250A>G (p.His2417Arg) rs147185142
NM_000426.3(LAMA2):c.7300+10T>A rs200469923
NM_000426.3(LAMA2):c.7300+19A>G rs115892449
NM_000426.3(LAMA2):c.7390G>T (p.Ala2464Ser) rs1131691621
NM_000426.3(LAMA2):c.7431A>T (p.Arg2477Ser) rs34367843
NM_000426.3(LAMA2):c.7440-9G>A rs369558532
NM_000426.3(LAMA2):c.7452-9A>G rs748647936
NM_000426.3(LAMA2):c.7479C>T (p.Ser2493=) rs368989339
NM_000426.3(LAMA2):c.74C>T (p.Pro25Leu) rs145310035
NM_000426.3(LAMA2):c.7536C>T (p.Pro2512=) rs778297793
NM_000426.3(LAMA2):c.7640G>A (p.Gly2547Glu) rs115488979
NM_000426.3(LAMA2):c.7680C>T (p.Ser2560=) rs750957928
NM_000426.3(LAMA2):c.7760T>C (p.Val2587Ala) rs2229848
NM_000426.3(LAMA2):c.7830G>C (p.Val2610=) rs2229849
NM_000426.3(LAMA2):c.7845G>A (p.Pro2615=) rs2229850
NM_000426.3(LAMA2):c.7906A>G (p.Thr2636Ala) rs2244008
NM_000426.3(LAMA2):c.7991delG (p.Gly2664Valfs) rs886039541
NM_000426.3(LAMA2):c.8028T>C (p.Asn2676=) rs35313209
NM_000426.3(LAMA2):c.8075+16C>T rs776913896
NM_000426.3(LAMA2):c.8076-15A>G rs368086451
NM_000426.3(LAMA2):c.8076-7C>G rs555377928
NM_000426.3(LAMA2):c.8124T>A (p.Gly2708=) rs34997144
NM_000426.3(LAMA2):c.8223G>A (p.Thr2741=) rs150596964
NM_000426.3(LAMA2):c.8244+13A>G rs1057523272
NM_000426.3(LAMA2):c.8245-2A>G rs914395925
NM_000426.3(LAMA2):c.8357+19C>T rs1057523035
NM_000426.3(LAMA2):c.8452C>G (p.Leu2818Val) rs1064795750
NM_000426.3(LAMA2):c.848T>C (p.Val283Ala) rs376917587
NM_000426.3(LAMA2):c.8528A>G (p.Asn2843Ser) rs73599293
NM_000426.3(LAMA2):c.8548-10T>C rs113644365
NM_000426.3(LAMA2):c.8586T>C (p.Tyr2862=) rs142451929
NM_000426.3(LAMA2):c.8637G>C (p.Leu2879=) rs370496870
NM_000426.3(LAMA2):c.8669dup (p.Leu2890Phefs) rs1554316216
NM_000426.3(LAMA2):c.8690G>A (p.Arg2897Gln) rs201696115
NM_000426.3(LAMA2):c.8691A>G (p.Arg2897=) rs2228599
NM_000426.3(LAMA2):c.8727C>T (p.Cys2909=) rs148285711
NM_000426.3(LAMA2):c.8755C>T (p.Pro2919Ser) rs143026295
NM_000426.3(LAMA2):c.8774C>T (p.Pro2925Leu) rs77113162
NM_000426.3(LAMA2):c.8842G>A (p.Gly2948Ser) rs143638361
NM_000426.3(LAMA2):c.8918C>T (p.Thr2973Met) rs145842163
NM_000426.3(LAMA2):c.8937G>C (p.Gly2979=) rs1194078171
NM_000426.3(LAMA2):c.9001G>C (p.Val3001Leu) rs189360899
NM_000426.3(LAMA2):c.9039T>C (p.Asp3013=) rs1057523899
NM_000426.3(LAMA2):c.9051A>G (p.Pro3017=) rs1057522162
NM_000426.3(LAMA2):c.910-14delC rs769173629
NM_000426.3(LAMA2):c.9123C>T (p.Val3041=) rs61749497
NM_000426.3(LAMA2):c.9145C>G (p.Gln3049Glu) rs146525742
NM_000426.3(LAMA2):c.917G>A (p.Arg306His) rs1023922833
NM_000426.3(LAMA2):c.9211+17C>T rs367830612
NM_000426.3(LAMA2):c.9212-11G>A rs770088527
NM_000426.3(LAMA2):c.9212-15C>A rs55776770
NM_000426.3(LAMA2):c.922G>A (p.Glu308Lys) rs146462599
NM_000426.3(LAMA2):c.9253C>T rs121913571
NM_000426.3(LAMA2):c.9269_9283dup (p.Thr3094_Lys3095insThrLeuLysLeuThr) rs1554321191
NM_000426.3(LAMA2):c.9339C>A (p.Gly3113=) rs182391310
NM_000426.3(LAMA2):c.9340G>A (p.Val3114Ile) rs200796753
NM_000426.3(LAMA2):c.946G>A (p.Asp316Asn) rs141340479
NM_000426.3(LAMA2):c.99A>G (p.Ala33=) rs762858697

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.