ClinVar Miner

List of variants in gene MYH9 reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_002473.6(MYH9):c.3429T>G (p.Ala1143=) rs710181 0.97278
NM_002473.6(MYH9):c.1728+10G>A rs2413396 0.77118
NM_002473.6(MYH9):c.1554+7A>G rs3752462 0.53193
NM_002473.6(MYH9):c.4876A>G (p.Ile1626Val) rs2269529 0.17342
NM_002473.6(MYH9):c.4872G>T (p.Ala1624=) rs2269530 0.17309
NM_002473.6(MYH9):c.4899G>A (p.Arg1633=) rs5756130 0.07263
NM_002473.6(MYH9):c.2256T>C (p.Asn752=) rs9619601 0.04672
NM_002473.6(MYH9):c.3345A>G (p.Glu1115=) rs875725 0.03292
NM_002473.6(MYH9):c.4563C>T (p.His1521=) rs11549907 0.02903
NM_002473.6(MYH9):c.3100+11G>C rs41279999 0.02869
NM_002473.6(MYH9):c.3838-8C>T rs145429636 0.02315
NM_002473.6(MYH9):c.3838-12C>T rs113698937 0.01529
NM_002473.6(MYH9):c.1626C>T (p.Phe542=) rs7285745 0.01011
NM_002473.6(MYH9):c.1108+9C>T rs145751072 0.00959
NM_002473.6(MYH9):c.2038-5T>C rs8137674 0.00874
NM_002473.6(MYH9):c.1729-6C>T rs9622375 0.00736
NM_002473.6(MYH9):c.136C>T (p.Leu46Phe) rs147122501 0.00554
NM_002473.6(MYH9):c.5815G>A (p.Ala1939Thr) rs115031369 0.00508
NM_002473.6(MYH9):c.1083C>T (p.Asp361=) rs56001030 0.00436
NM_002473.6(MYH9):c.1555-12C>T rs148641114 0.00392
NM_002473.6(MYH9):c.2229+13G>T rs139146113 0.00377
NM_002473.6(MYH9):c.5181G>A (p.Leu1727=) rs115170675 0.00292
NM_002473.6(MYH9):c.7C>G (p.Gln3Glu) rs56200894 0.00231
NM_002473.6(MYH9):c.4396C>T (p.Arg1466Trp) rs139134727 0.00195
NM_002473.6(MYH9):c.3485+8C>T rs149559551 0.00193
NM_002473.6(MYH9):c.4952T>C (p.Met1651Thr) rs142094977 0.00165
NM_002473.6(MYH9):c.5818G>A (p.Gly1940Arg) rs140588099 0.00156
NM_002473.6(MYH9):c.4198C>T (p.Arg1400Trp) rs76368635 0.00123
NM_002473.6(MYH9):c.1176G>A (p.Pro392=) rs143316848 0.00121
NM_002473.6(MYH9):c.705+11C>T rs201738304 0.00114
NM_002473.6(MYH9):c.2448C>T (p.Cys816=) rs113285582 0.00112
NM_002473.6(MYH9):c.4727G>A (p.Arg1576Gln) rs143269195 0.00088
NM_002473.6(MYH9):c.2517G>A (p.Gln839=) rs34498733 0.00038
NM_002473.6(MYH9):c.2061C>T (p.Leu687=) rs143801000 0.00022
NM_002473.6(MYH9):c.18C>T (p.Ala6=) rs141055332 0.00021
NM_002473.6(MYH9):c.3320G>A (p.Arg1107Gln) rs137924205 0.00004
NM_002473.6(MYH9):c.3697G>A (p.Val1233Met) rs542791128 0.00001
NM_002473.6(MYH9):c.255C>T (p.Asp85=) rs569718443
NM_002473.6(MYH9):c.5275-10del rs552643559
NM_002473.6(MYH9):c.5483+4C>G rs56327920
NM_002473.6(MYH9):c.5593-14G>T rs201676960
NM_002473.6(MYH9):c.5766-3del rs141686520
NM_002473.6(MYH9):c.5781G>T (p.Pro1927=) rs80050551

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