ClinVar Miner

List of variants in gene MSH6 reported as uncertain significance by PreventionGenetics

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Total variants: 27
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HGVS dbSNP
NM_000179.2(MSH6):c.*1A>G rs587781604
NM_000179.2(MSH6):c.1120_1122del (p.Lys374del) rs587781660
NM_000179.2(MSH6):c.1402C>T (p.Arg468Cys) rs369456858
NM_000179.2(MSH6):c.1474A>G (p.Met492Val) rs61754783
NM_000179.2(MSH6):c.1602C>G (p.Asn534Lys) rs763712971
NM_000179.2(MSH6):c.1915G>A (p.Glu639Lys) rs143517321
NM_000179.2(MSH6):c.19C>A (p.Leu7Met) rs1064795094
NM_000179.2(MSH6):c.19C>G (p.Leu7Val) rs1064795094
NM_000179.2(MSH6):c.2006T>C (p.Ile669Thr) rs555209664
NM_000179.2(MSH6):c.2145C>G (p.Asp715Glu) rs1221484522
NM_000179.2(MSH6):c.2398G>C (p.Val800Leu) rs61748083
NM_000179.2(MSH6):c.2419G>A (p.Glu807Lys) rs587779923
NM_000179.2(MSH6):c.2561A>T (p.Lys854Met) rs34374438
NM_000179.2(MSH6):c.2920A>G (p.Arg974Gly) rs775407589
NM_000179.2(MSH6):c.3151G>A (p.Val1051Ile) rs576269342
NM_000179.2(MSH6):c.3203G>A (p.Arg1068Gln) rs398123230
NM_000179.2(MSH6):c.3203G>C (p.Arg1068Pro) rs398123230
NM_000179.2(MSH6):c.3217C>T (p.Pro1073Ser) rs142254875
NM_000179.2(MSH6):c.3245C>T (p.Pro1082Leu) rs191109849
NM_000179.2(MSH6):c.3260C>A (p.Pro1087His) rs63750753
NM_000179.2(MSH6):c.33C>G (p.Phe11Leu) rs747802641
NM_000179.2(MSH6):c.3478G>A (p.Val1160Ile) rs376799914
NM_000179.2(MSH6):c.3727A>T (p.Thr1243Ser) rs147453999
NM_000179.2(MSH6):c.38A>G (p.Lys13Arg) rs41294988
NM_000179.2(MSH6):c.3961A>G (p.Arg1321Gly) rs41295278
NM_000179.2(MSH6):c.648_649delinsTT (p.Asp217Tyr) rs63750471
NM_000179.2(MSH6):c.984C>G (p.Ser328Arg) rs138143769

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