ClinVar Miner

List of variants in gene MSH2 reported as likely pathogenic by Counsyl

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Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_000251.2(MSH2):c.1046C>G (p.Pro349Arg) rs587779067
NM_000251.2(MSH2):c.1276+2T>C rs267607953
NM_000251.2(MSH2):c.301_306del (p.Glu101_Val102del) rs587779157
NM_000251.2(MSH2):c.354T>G (p.Tyr118Ter) rs1553350250
NM_000251.2(MSH2):c.806C>A (p.Ser269Ter) rs63750058
NM_000251.2(MSH2):c.943-2A>G rs587779198

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