ClinVar Miner

List of variants in gene MYH6 reported as uncertain significance by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_002471.4(MYH6):c.2579G>A (p.Arg860His) rs115845031 0.00573
NM_002471.4(MYH6):c.3010G>T (p.Ala1004Ser) rs143978652 0.00110
NM_002471.4(MYH6):c.831G>T (p.Gln277His) rs140660481 0.00029
NM_002471.4(MYH6):c.2401A>G (p.Ile801Val) rs75487328 0.00028
NM_002471.4(MYH6):c.4505G>A (p.Arg1502Gln) rs199936506 0.00022
NM_002471.4(MYH6):c.3383G>A (p.Arg1128His) rs376002621 0.00021
NM_002471.4(MYH6):c.4328C>A (p.Ala1443Asp) rs727503234 0.00019
NM_002471.4(MYH6):c.824T>A (p.Ile275Asn) rs201327273 0.00019
NM_002471.4(MYH6):c.5293G>A (p.Ala1765Thr) rs397516775 0.00016
NM_002471.4(MYH6):c.3195G>C (p.Gln1065His) rs267606904 0.00015
NM_002471.4(MYH6):c.1753G>A (p.Gly585Ser) rs150415679 0.00014
NM_002471.4(MYH6):c.5519A>G (p.Lys1840Arg) rs373629059 0.00011
NM_002471.4(MYH6):c.4264C>T (p.Arg1422Trp) rs200465713 0.00010
NM_002471.4(MYH6):c.1702C>T (p.Arg568Cys) rs149650190 0.00006
NM_002471.4(MYH6):c.5257G>C (p.Ala1753Pro) rs142437308 0.00006
NM_002471.4(MYH6):c.3347G>A (p.Arg1116His) rs369247906 0.00005
NM_002471.4(MYH6):c.5594G>A (p.Arg1865Gln) rs138720701 0.00004
NM_002471.4(MYH6):c.1108C>T (p.Arg370Trp) rs753444140 0.00003
NM_002471.4(MYH6):c.5348G>A (p.Arg1783His) rs745473249 0.00003
NM_002471.4(MYH6):c.5593C>T (p.Arg1865Trp) rs759499155 0.00003
NM_002471.4(MYH6):c.3135G>T (p.Lys1045Asn) rs758449996 0.00002
NM_002471.4(MYH6):c.2589G>C (p.Glu863Asp) rs763692915 0.00001
NM_002471.4(MYH6):c.4369G>A (p.Glu1457Lys) rs267606905 0.00001
NM_002471.4(MYH6):c.5278G>A (p.Ala1760Thr) rs146539406 0.00001
NM_002471.4(MYH6):c.1922A>T (p.Lys641Ile) rs1401348638
NM_002471.4(MYH6):c.2091C>A (p.Cys697Ter) rs1891418103
NM_002471.4(MYH6):c.2098G>T (p.Val700Leu) rs767142932
NM_002471.4(MYH6):c.2500C>T (p.Leu834Phe) rs1314476937
NM_002471.4(MYH6):c.4060G>A (p.Glu1354Lys) rs1595052281
NM_002471.4(MYH6):c.4144A>G (p.Ile1382Val) rs1555333536
NM_002471.4(MYH6):c.4265G>T (p.Arg1422Leu) rs574433291
NM_002471.4(MYH6):c.4595G>T (p.Arg1532Leu) rs34330111
NM_002471.4(MYH6):c.4645G>A (p.Ala1549Thr) rs1342437470
NM_002471.4(MYH6):c.5476_5477delinsAA (p.Gly1826Asn) rs878854502

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