ClinVar Miner

List of variants in gene MYH7 reported as likely benign by Preventiongenetics, part of Exact Sciences

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Gene type:
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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_000257.4(MYH7):c.2044+39A>T rs3729817 0.01368
NM_000257.4(MYH7):c.1408-42del rs45490796 0.01363
NM_000257.4(MYH7):c.2162+4G>A rs145738465 0.00276
NM_000257.4(MYH7):c.1579-47C>T rs45525037 0.00208
NM_000257.4(MYH7):c.3036C>T (p.Ala1012=) rs145379951 0.00050
NM_000257.4(MYH7):c.2145C>T (p.Tyr715=) rs146675572 0.00006
NM_000257.4(MYH7):c.1323G>A (p.Thr441=) rs397516096 0.00005
NM_000257.4(MYH7):c.1266T>C (p.Tyr422=) rs141519877 0.00004
NM_000257.4(MYH7):c.3666C>T (p.Ser1222=) rs397516191 0.00003
NM_000257.4(MYH7):c.3726+17C>T rs377463081 0.00003
NM_000257.4(MYH7):c.5736C>T (p.Ile1912=) rs200728597 0.00002
NM_000257.4(MYH7):c.5519T>C (p.Met1840Thr) rs149193520 0.00001
NM_000257.4(MYH7):c.797-17T>C rs532401716 0.00001
NM_000257.4(MYH7):c.870G>A (p.Leu290=) rs777259259 0.00001
NM_000257.4(MYH7):c.3337-4dup rs45504498
NM_000257.4(MYH7):c.797-19_797-17del rs372245426
NM_000257.4(MYH7):c.895+12C>A rs186276057

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