ClinVar Miner

List of variants in gene MSH2 reported as uncertain significance by Department of Pathology and Laboratory Medicine,Sinai Health System

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Gene type:
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Total variants: 16
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HGVS dbSNP
NM_000251.2(MSH2):c.1012G>A (p.Gly338Arg) rs63751004
NM_000251.2(MSH2):c.1277-12A>T rs1181142850
NM_000251.2(MSH2):c.1277-13T>A rs1553361114
NM_000251.2(MSH2):c.1805T>C (p.Leu602Pro) rs1553368561
NM_000251.2(MSH2):c.1825G>C (p.Ala609Pro) rs150980616
NM_000251.2(MSH2):c.1937A>G (p.Asp646Gly) rs41295290
NM_000251.2(MSH2):c.2027C>T (p.Ser676Leu) rs1057520735
NM_000251.2(MSH2):c.2075G>A (p.Gly692Glu) rs63751432
NM_000251.2(MSH2):c.2087C>T (p.Pro696Leu) rs267607994
NM_000251.2(MSH2):c.2178G>C (p.Met726Ile) rs587782396
NM_000251.2(MSH2):c.2266_2267insAGA (p.Thr756_Tyr757insLys) rs1553369686
NM_000251.2(MSH2):c.2785C>T (p.Arg929Ter) rs551060742
NM_000251.2(MSH2):c.2801C>A (p.Thr934Lys) rs587779969
NM_000251.2(MSH2):c.380A>G (p.Asn127Ser) rs17217772
NM_000251.2(MSH2):c.490G>T (p.Gly164Trp) rs63750582
NM_000251.2(MSH2):c.731T>C (p.Leu244Ser) rs1553351657

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