ClinVar Miner

List of variants in gene MSH2 reported as benign for Lynch syndrome

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Total variants: 52
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HGVS dbSNP
NM_000251.2(MSH2):c.*129T>C rs587779059
NM_000251.2(MSH2):c.*251+2441A>C rs6544991
NM_000251.2(MSH2):c.*272+4059G>A rs6720549
NM_000251.2(MSH2):c.-118T>C rs2303425
NM_000251.2(MSH2):c.-68-365T>G rs1863332
NM_000251.2(MSH2):c.1076+3400C>T rs4952887
NM_000251.2(MSH2):c.1077-10T>C rs17224360
NM_000251.2(MSH2):c.1077-2037G>T rs13425206
NM_000251.2(MSH2):c.1077-80G>A rs2347794
NM_000251.2(MSH2):c.1168C>T (p.Leu390Phe) rs17224367
NM_000251.2(MSH2):c.1276+51C>A rs17217961
NM_000251.2(MSH2):c.1276+6765G>A rs3771274
NM_000251.2(MSH2):c.1277-118G>A rs1981929
NM_000251.2(MSH2):c.1277-212T>A rs1981928
NM_000251.2(MSH2):c.1277-5849T>C rs17036577
NM_000251.2(MSH2):c.1277-6990T>G rs13408008
NM_000251.2(MSH2):c.1277-945A>C rs7607312
NM_000251.2(MSH2):c.1387-250G>A rs6741393
NM_000251.2(MSH2):c.1387-8G>T rs187525243
NM_000251.2(MSH2):c.1511-1516C>T rs3771281
NM_000251.2(MSH2):c.1511-91G>T rs3732182
NM_000251.2(MSH2):c.1511-9A>T rs12998837
NM_000251.2(MSH2):c.1661+12G>A rs3732183
NM_000251.2(MSH2):c.1661+90T>C rs10183143
NM_000251.2(MSH2):c.1662-9G>A rs17218356
NM_000251.2(MSH2):c.1666T>C (p.Leu556=) rs61756466
NM_000251.2(MSH2):c.1690A>G (p.Thr564Ala) rs55778204
NM_000251.2(MSH2):c.1737A>G (p.Lys579=) rs61756467
NM_000251.2(MSH2):c.1759+501A>G rs17036614
NM_000251.2(MSH2):c.1760-62G>A rs17218439
NM_000251.2(MSH2):c.1886A>G (p.Gln629Arg) rs61756468
NM_000251.2(MSH2):c.2006-265A>G rs2059520
NM_000251.2(MSH2):c.2006-6T>C rs2303428
NM_000251.2(MSH2):c.211+98T>C rs3815865
NM_000251.2(MSH2):c.211+9C>G rs2303426
NM_000251.2(MSH2):c.2205C>A (p.Ile735=) rs533553381
NM_000251.2(MSH2):c.2210+274T>G rs4608577
NM_000251.2(MSH2):c.2210+317G>C rs4638843
NM_000251.2(MSH2):c.2355T>C (p.His785=) rs1114167840
NM_000251.2(MSH2):c.23C>T (p.Thr8Met) rs17217716
NM_000251.2(MSH2):c.2635-214T>C rs2042649
NM_000251.2(MSH2):c.279_281delTCT rs267607919
NM_000251.2(MSH2):c.317G>A (p.Arg106Lys) rs41295286
NM_000251.2(MSH2):c.339G>A (p.Lys113=) rs35898375
NM_000251.2(MSH2):c.380A>G (p.Asn127Ser) rs17217772
NM_000251.2(MSH2):c.573C>T (p.Leu191=) rs1800151
NM_000251.2(MSH2):c.593A>G (p.Glu198Gly) rs63750327
NM_000251.2(MSH2):c.7G>T (p.Val3Leu) rs1257347271
NM_000251.2(MSH2):c.815C>T (p.Ala272Val) rs34136999
NM_000251.2(MSH2):c.942+17_942+29del rs11309117
NM_000251.2(MSH2):c.965G>A (p.Gly322Asp) rs4987188
NM_001258281.1(MSH2):c.744+25_744+29del rs11309117

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