ClinVar Miner

List of variants in gene MYH7 reported as likely benign for Cardiovascular phenotype

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Total variants: 58
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HGVS dbSNP
NM_000257.4(MYH7):c.1119G>A (p.Ala373=) rs572672362
NM_000257.4(MYH7):c.1191G>A (p.Lys397=) rs139506719
NM_000257.4(MYH7):c.1230C>T (p.Tyr410=) rs150885220
NM_000257.4(MYH7):c.1301G>A (p.Arg434Lys) rs786205356
NM_000257.4(MYH7):c.1323G>A (p.Thr441=) rs397516096
NM_000257.4(MYH7):c.1395C>T (p.Phe465=) rs45508293
NM_000257.4(MYH7):c.153C>T (p.Ile51=) rs373145667
NM_000257.4(MYH7):c.1632C>T (p.Thr544=) rs587781089
NM_000257.4(MYH7):c.1671G>A (p.Leu557=) rs149386750
NM_000257.4(MYH7):c.1755C>A (p.Ile585=) rs201860580
NM_000257.4(MYH7):c.2091T>C (p.Gly697=) rs140380523
NM_000257.4(MYH7):c.2162+4G>A rs145738465
NM_000257.4(MYH7):c.2334C>T (p.Asp778=) rs2069544
NM_000257.4(MYH7):c.2349C>T (p.Arg783=) rs139882431
NM_000257.4(MYH7):c.2358G>T (p.Thr786=) rs36211714
NM_000257.4(MYH7):c.2526T>C (p.Ser842=) rs554560162
NM_000257.4(MYH7):c.261C>T (p.Ile87=) rs148560996
NM_000257.4(MYH7):c.2769C>T (p.Asn923=) rs36211716
NM_000257.4(MYH7):c.2877G>A (p.Leu959=) rs886039162
NM_000257.4(MYH7):c.2907C>T (p.His969=) rs142573531
NM_000257.4(MYH7):c.2931C>T (p.Asn977=) rs757313728
NM_000257.4(MYH7):c.3036C>T (p.Ala1012=) rs145379951
NM_000257.4(MYH7):c.3156G>A (p.Lys1052=) rs138294643
NM_000257.4(MYH7):c.3240G>A (p.Leu1080=) rs776886972
NM_000257.4(MYH7):c.3261G>A (p.Leu1087=) rs371937608
NM_000257.4(MYH7):c.3273C>T (p.Asn1091=) rs200664031
NM_000257.4(MYH7):c.327C>T (p.Tyr109=) rs36211408
NM_000257.4(MYH7):c.3639G>A (p.Val1213=) rs1238904908
NM_000257.4(MYH7):c.3648G>A (p.Lys1216=) rs1555337101
NM_000257.4(MYH7):c.3682C>T (p.Leu1228=) rs560995739
NM_000257.4(MYH7):c.3789G>A (p.Ala1263=) rs137918672
NM_000257.4(MYH7):c.3846C>G (p.Thr1282=) rs948996596
NM_000257.4(MYH7):c.3918C>T (p.Leu1306=) rs144420313
NM_000257.4(MYH7):c.3981C>A (p.Asn1327Lys) rs141764279
NM_000257.4(MYH7):c.4005G>A (p.Ser1335=) rs144465613
NM_000257.4(MYH7):c.4083T>G (p.Leu1361=) rs754295295
NM_000257.4(MYH7):c.4134C>T (p.Asp1378=) rs770630028
NM_000257.4(MYH7):c.4158C>T (p.Leu1386=) rs886050418
NM_000257.4(MYH7):c.4188G>A (p.Arg1396=) rs200852418
NM_000257.4(MYH7):c.453G>A (p.Pro151=) rs777382773
NM_000257.4(MYH7):c.5245A>C (p.Arg1749=) rs562465062
NM_000257.4(MYH7):c.5253T>C (p.Ala1751=) rs776282574
NM_000257.4(MYH7):c.540C>A (p.Ser180=) rs369490861
NM_000257.4(MYH7):c.5412C>G (p.Ala1804=) rs147433856
NM_000257.4(MYH7):c.5421C>T (p.Gly1807=) rs142844109
NM_000257.4(MYH7):c.5481G>A (p.Glu1827=) rs368848344
NM_000257.4(MYH7):c.5484C>T (p.Ala1828=) rs202175645
NM_000257.4(MYH7):c.5499C>T (p.Asn1833=) rs3729831
NM_000257.4(MYH7):c.5562G>A (p.Thr1854=) rs368706722
NM_000257.4(MYH7):c.5727G>A (p.Arg1909=) rs761750159
NM_000257.4(MYH7):c.5736C>T (p.Ile1912=) rs200728597
NM_000257.4(MYH7):c.705C>T (p.Thr235=) rs552415639
NM_000257.4(MYH7):c.714C>T (p.Asn238=) rs202141819
NM_000257.4(MYH7):c.77C>T (p.Ala26Val) rs186964570
NM_000257.4(MYH7):c.924C>T (p.Tyr308=) rs762065412
NM_000257.4(MYH7):c.930T>C (p.Tyr310=) rs111626355
NM_000257.4(MYH7):c.954C>G (p.Thr318=) rs773934091
NM_000257.4(MYH7):c.957C>T (p.Thr319=) rs368699342

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