ClinVar Miner

List of variants in gene MSH2 reported as benign by Mendelics

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Gene type:
ClinVar version:
Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_000251.2(MSH2):c.-118T>C rs2303425 0.10354
NM_000251.3(MSH2):c.1511-9A>T rs12998837 0.09123
NM_000251.3(MSH2):c.23C>T (p.Thr8Met) rs17217716 0.00184
NM_000251.3(MSH2):c.55T>C (p.Phe19Leu) rs141711342 0.00063
NM_000251.3(MSH2):c.1563T>C (p.Tyr521=) rs63750330 0.00053
NM_000251.3(MSH2):c.815C>T (p.Ala272Val) rs34136999 0.00046
NM_000251.3(MSH2):c.1511-41G>C rs202215396 0.00038
NM_000251.3(MSH2):c.1255C>A (p.Gln419Lys) rs63750006 0.00019
NM_000251.3(MSH2):c.1730T>C (p.Ile577Thr) rs63749910 0.00018
NM_000251.3(MSH2):c.1690A>G (p.Thr564Ala) rs55778204 0.00008
NM_000251.3(MSH2):c.499G>C (p.Asp167His) rs63750255 0.00006
NM_000251.3(MSH2):c.459C>T (p.Ser153=) rs63751065 0.00001
NM_000251.3(MSH2):c.2005+59_2005+61dup rs76761634
NM_000251.3(MSH2):c.2276G>A (p.Gly759Glu) rs386833406
NM_000251.3(MSH2):c.2575G>A (p.Glu859Lys) rs63749830
NM_000251.3(MSH2):c.2714C>G (p.Thr905Arg) rs267608022
NM_000251.3(MSH2):c.273TCT[2] (p.Leu94del) rs267607919
NM_000251.3(MSH2):c.593A>G (p.Glu198Gly) rs63750327
NM_000251.3(MSH2):c.67T>C (p.Phe23Leu) rs372619120
NM_000251.3(MSH2):c.942+10_942+29dup rs11309117
NM_000251.3(MSH2):c.942+11_942+29dup rs11309117
NM_000251.3(MSH2):c.942+12_942+29dup rs11309117
NM_000251.3(MSH2):c.942+13_942+29dup rs11309117
NM_000251.3(MSH2):c.942+14_942+29dup rs11309117
NM_000251.3(MSH2):c.942+15_942+29dup rs11309117
NM_000251.3(MSH2):c.942+16_942+29dup rs11309117
NM_000251.3(MSH2):c.942+17_942+29dup rs11309117
NM_000251.3(MSH2):c.942+18_942+29dup rs11309117
NM_000251.3(MSH2):c.942+19_942+29dup rs11309117
NM_000251.3(MSH2):c.942+20_942+29dup rs11309117
NM_000251.3(MSH2):c.942+21_942+29dup rs11309117
NM_000251.3(MSH2):c.942+22_942+29del rs11309117
NM_000251.3(MSH2):c.942+22_942+29dup rs11309117
NM_000251.3(MSH2):c.942+23_942+29del rs11309117
NM_000251.3(MSH2):c.942+23_942+29dup rs11309117
NM_000251.3(MSH2):c.942+24_942+29del rs11309117
NM_000251.3(MSH2):c.942+24_942+29dup rs11309117
NM_000251.3(MSH2):c.942+25_942+29dup rs11309117
NM_000251.3(MSH2):c.942+26_942+29del rs11309117
NM_000251.3(MSH2):c.942+26_942+29dup rs11309117
NM_000251.3(MSH2):c.942+27_942+29del rs11309117
NM_000251.3(MSH2):c.942+27_942+29dup rs11309117
NM_000251.3(MSH2):c.942+28_942+29dup rs11309117
NM_000251.3(MSH2):c.942+29del rs11309117
NM_000251.3(MSH2):c.942+29dup rs11309117
NM_000251.3(MSH2):c.942+7_942+29dup rs11309117
NM_000251.3(MSH2):c.942+8_942+29dup rs11309117
NM_000251.3(MSH2):c.942+9_942+29dup rs11309117

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