ClinVar Miner

List of variants in gene MYH6 reported as uncertain significance by Biesecker Lab/Clinical Genomics Section,National Institutes of Health

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Gene type:
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Total variants: 20
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HGVS dbSNP
NM_002471.3(MYH6):c.1252G>A (p.Val418Met) rs147606900
NM_002471.3(MYH6):c.1328G>A (p.Arg443His) rs202096001
NM_002471.3(MYH6):c.1716dup (p.Lys573fs) rs786205354
NM_002471.3(MYH6):c.2575G>T (p.Gly859Trp) rs369274077
NM_002471.3(MYH6):c.3195G>C (p.Gln1065His) rs267606904
NM_002471.3(MYH6):c.3346C>A (p.Arg1116Ser) rs372446459
NM_002471.3(MYH6):c.3448G>A (p.Glu1150Lys) rs760399050
NM_002471.3(MYH6):c.3817A>T (p.Asn1273Tyr) rs200503588
NM_002471.3(MYH6):c.3988G>A (p.Ala1330Thr) rs757840030
NM_002471.3(MYH6):c.4026C>A (p.Cys1342Ter) rs141062252
NM_002471.3(MYH6):c.4193G>A (p.Arg1398Gln) rs150815925
NM_002471.3(MYH6):c.4429C>T (p.Arg1477Cys) rs201989347
NM_002471.3(MYH6):c.4505G>A (p.Arg1502Gln) rs199936506
NM_002471.3(MYH6):c.4772A>G (p.Asn1591Ser) rs200751434
NM_002471.3(MYH6):c.4822C>T (p.Arg1608Cys) rs201683868
NM_002471.3(MYH6):c.5135G>T (p.Ser1712Ile) rs201383498
NM_002471.3(MYH6):c.5140C>T (p.Arg1714Trp) rs140651265
NM_002471.3(MYH6):c.731G>A (p.Arg244His) rs200645920
NM_002471.3(MYH6):c.824T>A (p.Ile275Asn) rs201327273
NM_002471.3(MYH6):c.831G>T (p.Gln277His) rs140660481

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