ClinVar Miner

List of variants in gene combination LOC126861896, MYH6 reported by GeneDx

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Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_002471.4(MYH6):c.4914T>C (p.Ala1638=) rs178640 0.52673
NM_002471.4(MYH6):c.4651-17G>A rs2071634 0.23331
NM_002471.4(MYH6):c.4980C>T (p.Asp1660=) rs382872 0.07604
NM_002471.4(MYH6):c.4960-17A>T rs28730764 0.03950
NM_002471.4(MYH6):c.4838T>C (p.Val1613Ala) rs61742476 0.03922
NM_002471.4(MYH6):c.4778A>T (p.Gln1593Leu) rs45574136 0.03743
NM_002471.4(MYH6):c.4959+13G>A rs28730765 0.00762
NM_002471.4(MYH6):c.4899C>T (p.His1633=) rs61742474 0.00517
NM_002471.4(MYH6):c.4651-12A>C rs193922653 0.00399
NM_002471.4(MYH6):c.4782G>A (p.Arg1594=) rs142823394 0.00125
NM_002471.4(MYH6):c.4906C>T (p.Arg1636Cys) rs149460065 0.00113
NM_002471.4(MYH6):c.4986G>A (p.Ala1662=) rs77416370 0.00079
NM_002471.4(MYH6):c.4905C>T (p.Asn1635=) rs143048583 0.00043
NM_002471.4(MYH6):c.5140C>A (p.Arg1714=) rs140651265 0.00036
NM_002471.4(MYH6):c.5112G>A (p.Ala1704=) rs150450178 0.00031
NM_002471.4(MYH6):c.4960-9G>A rs557113705 0.00029
NM_002471.4(MYH6):c.4772A>G (p.Asn1591Ser) rs200751434 0.00022
NM_002471.4(MYH6):c.4812T>C (p.Asp1604=) rs201667127 0.00016
NM_002471.4(MYH6):c.4651-3C>A rs572175190 0.00009
NM_002471.4(MYH6):c.4727G>A (p.Arg1576Gln) rs771898553 0.00008
NM_002471.4(MYH6):c.4747G>A (p.Glu1583Lys) rs397516771 0.00008
NM_002471.4(MYH6):c.4833C>T (p.Asn1611=) rs139329956 0.00008
NM_002471.4(MYH6):c.5085G>A (p.Glu1695=) rs1206016022 0.00008
NM_002471.4(MYH6):c.4991G>A (p.Arg1664His) rs778287981 0.00006
NM_002471.4(MYH6):c.5102G>A (p.Arg1701Gln) rs762103586 0.00006
NM_002471.4(MYH6):c.5026G>A (p.Val1676Met) rs773755388 0.00005
NM_002471.4(MYH6):c.5077G>A (p.Val1693Met) rs373457153 0.00005
NM_002471.4(MYH6):c.5095C>T (p.Arg1699Trp) rs766345714 0.00005
NM_002471.4(MYH6):c.4822C>T (p.Arg1608Cys) rs201683868 0.00004
NM_002471.4(MYH6):c.4993G>A (p.Ala1665Thr) rs374271404 0.00004
NM_002471.4(MYH6):c.4750G>A (p.Glu1584Lys) rs1280321639 0.00003
NM_002471.4(MYH6):c.4768C>A (p.Arg1590Ser) rs544624250 0.00003
NM_002471.4(MYH6):c.4829G>A (p.Arg1610His) rs758792342 0.00003
NM_002471.4(MYH6):c.4959+12C>T rs371661383 0.00003
NM_002471.4(MYH6):c.5137G>A (p.Glu1713Lys) rs369275573 0.00003
NM_002471.4(MYH6):c.4793C>T (p.Ser1598Leu) rs536807961 0.00002
NM_002471.4(MYH6):c.4981G>A (p.Asp1661Asn) rs771357562 0.00002
NM_002471.4(MYH6):c.5035C>T (p.Arg1679Cys) rs921540558 0.00002
NM_002471.4(MYH6):c.4781G>A (p.Arg1594Gln) rs146095234 0.00001
NM_002471.4(MYH6):c.4798C>A (p.Gln1600Lys) rs770068575 0.00001
NM_002471.4(MYH6):c.4823G>A (p.Arg1608His) rs747494958 0.00001
NM_002471.4(MYH6):c.4834G>A (p.Glu1612Lys) rs1417882969 0.00001
NM_002471.4(MYH6):c.4874A>G (p.Asn1625Ser) rs776765616 0.00001
NM_002471.4(MYH6):c.4900G>A (p.Ala1634Thr) rs369767936 0.00001
NM_002471.4(MYH6):c.4949G>A (p.Ser1650Asn) rs767073355 0.00001
NM_002471.4(MYH6):c.5033G>A (p.Arg1678Gln) rs141195890 0.00001
NM_002471.4(MYH6):c.5072G>A (p.Arg1691His) rs727504502 0.00001
NM_002471.4(MYH6):c.4661A>T (p.Glu1554Val) rs2502144371
NM_002471.4(MYH6):c.4665C>A (p.His1555Gln) rs373888186
NM_002471.4(MYH6):c.4665C>T (p.His1555=) rs373888186
NM_002471.4(MYH6):c.4752_4753delinsAT (p.Met1585Leu) rs2502143923
NM_002471.4(MYH6):c.4759C>T (p.Gln1587Ter) rs2502143899
NM_002471.4(MYH6):c.4786G>T (p.Val1596Leu)
NM_002471.4(MYH6):c.4925A>C (p.Gln1642Pro) rs1487346307
NM_002471.4(MYH6):c.4942C>T (p.Leu1648Phe) rs2502143068
NM_002471.4(MYH6):c.4955T>C (p.Leu1652Pro) rs2138584834
NM_002471.4(MYH6):c.5002G>C (p.Asp1668His) rs200884672
NM_002471.4(MYH6):c.5136C>A (p.Ser1712Arg) rs397516774
NM_002471.4(MYH6):c.5136C>G (p.Ser1712Arg) rs397516774
NM_002471.4(MYH6):c.5163+3G>A rs1057524287

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