ClinVar Miner

List of variants in gene MYH7 reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Gene type:
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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_000257.4(MYH7):c.3972+62_3972+63insC rs34598192 0.42217
NM_000257.4(MYH7):c.2890G>C (p.Val964Leu) rs45496496 0.00050
NM_000257.4(MYH7):c.3382G>A (p.Ala1128Thr) rs199552354 0.00011
NM_000257.4(MYH7):c.5329G>A (p.Ala1777Thr) rs200939753 0.00009
NM_000257.4(MYH7):c.5326A>G (p.Ser1776Gly) rs369437262 0.00006
NM_000257.4(MYH7):c.968T>C (p.Ile323Thr) rs397516275 0.00006
NM_000257.4(MYH7):c.5559+4C>T rs727504319 0.00005
NM_000257.4(MYH7):c.211G>A (p.Val71Met) rs730880830 0.00004
NM_000257.4(MYH7):c.5790+14T>A rs370553746 0.00004
NM_000257.4(MYH7):c.5471A>G (p.Asn1824Ser) rs760218400 0.00003
NM_000257.4(MYH7):c.11C>T (p.Ser4Leu) rs758659692 0.00002
NM_000257.4(MYH7):c.3301G>A (p.Gly1101Ser) rs367546859 0.00002
NM_000257.4(MYH7):c.3854-5C>T rs752385694 0.00002
NM_000257.4(MYH7):c.4076G>A (p.Arg1359His) rs750836033 0.00002
NM_000257.4(MYH7):c.5537G>A (p.Arg1846His) rs757803046 0.00002
NM_000257.4(MYH7):c.1699C>T (p.Arg567Cys) rs771771163 0.00001
NM_000257.4(MYH7):c.201+13C>T rs781529698 0.00001
NM_000257.4(MYH7):c.2044+18G>A rs1406715881 0.00001
NM_000257.4(MYH7):c.2286+7A>G rs758365123 0.00001
NM_000257.4(MYH7):c.2286G>A (p.Lys762=) rs958169569 0.00001
NM_000257.4(MYH7):c.22G>A (p.Val8Ile) rs754388460 0.00001
NM_000257.4(MYH7):c.2908G>A (p.Ala970Thr) rs1446657813 0.00001
NM_000257.4(MYH7):c.3245+2T>G rs113859723 0.00001
NM_000257.4(MYH7):c.3337G>A (p.Ala1113Thr) rs193922388 0.00001
NM_000257.4(MYH7):c.3407G>A (p.Arg1136His) rs730880905 0.00001
NM_000257.4(MYH7):c.3551A>T (p.Gln1184Leu) rs546586969 0.00001
NM_000257.4(MYH7):c.3781A>C (p.Ser1261Arg) rs193922389 0.00001
NM_000257.4(MYH7):c.3883G>A (p.Glu1295Lys) rs730880785 0.00001
NM_000257.4(MYH7):c.5341C>T (p.Arg1781Cys) rs397516245 0.00001
NM_000257.4(MYH7):c.5519T>C (p.Met1840Thr) rs149193520 0.00001
NM_000257.4(MYH7):c.1048T>C (p.Tyr350His) rs730880863
NM_000257.4(MYH7):c.1061G>A (p.Gly354Asp) rs2138677416
NM_000257.4(MYH7):c.1225G>A (p.Glu409Lys) rs1892823735
NM_000257.4(MYH7):c.12_24del (p.Glu5fs)
NM_000257.4(MYH7):c.1588A>G (p.Ile530Val) rs771831848
NM_000257.4(MYH7):c.193T>C (p.Tyr65His) rs2138686468
NM_000257.4(MYH7):c.1956+20A>C rs774605900
NM_000257.4(MYH7):c.200A>C (p.Lys67Thr) rs2138686446
NM_000257.4(MYH7):c.2923-5G>A rs779010466
NM_000257.4(MYH7):c.2997del (p.Gln1000fs) rs2138662562
NM_000257.4(MYH7):c.3336+20G>T
NM_000257.4(MYH7):c.3748C>T (p.Arg1250Trp) rs727503249
NM_000257.4(MYH7):c.3981C>A (p.Asn1327Lys) rs141764279
NM_000257.4(MYH7):c.4144C>T (p.Arg1382Trp) rs730880910
NM_000257.4(MYH7):c.520A>G (p.Ile174Val)
NM_000257.4(MYH7):c.5365A>G (p.Thr1789Ala)
NM_000257.4(MYH7):c.5395G>A (p.Glu1799Lys) rs730880816
NM_000257.4(MYH7):c.5470_5471delinsGG (p.Asn1824Gly) rs1595071680
NM_000257.4(MYH7):c.5654C>G (p.Ala1885Gly) rs1892080169
NM_000257.4(MYH7):c.5704G>A (p.Glu1902Lys) rs187073962
NM_000257.4(MYH7):c.641G>A (p.Gly214Asp)
NM_000257.4(MYH7):c.692G>T (p.Gly231Val) rs1380372471
NM_000257.4(MYH7):c.704C>A (p.Thr235Asn) rs1892944195
NM_000257.4(MYH7):c.953C>A (p.Thr318Asn) rs397516274

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