ClinVar Miner

List of variants in gene combination MYH11, NDE1 reported as likely benign for Cardiovascular phenotype

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Total variants: 30
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HGVS dbSNP
NM_001040113.1(MYH11):c.4218G>A (p.Lys1406=) rs113302393
NM_001040113.1(MYH11):c.4625G>A (p.Arg1542Gln) rs137934837
NM_001040113.1(MYH11):c.5357C>T (p.Thr1786Met) rs201960644
NM_001040114.1(MYH11):c.4694C>T (p.Thr1565Met) rs111854563
NM_001143979.1(NDE1):c.948-5807C>G rs144421849
NM_002474.2(MYH11):c.4239C>T (p.Ala1413=) rs138573101
NM_002474.2(MYH11):c.4240G>A (p.Ala1414Thr) rs112467954
NM_002474.2(MYH11):c.4353G>A (p.Arg1451=) rs1463240400
NM_002474.2(MYH11):c.4578+3A>G rs143288748
NM_002474.2(MYH11):c.4638G>A (p.Thr1546=) rs141314621
NM_002474.2(MYH11):c.4680C>T (p.Asp1560=) rs142613263
NM_002474.2(MYH11):c.4774A>C (p.Arg1592=) rs114556043
NM_002474.2(MYH11):c.4809G>A (p.Thr1603=) rs140577744
NM_002474.2(MYH11):c.4884C>T (p.Asp1628=) rs780786328
NM_002474.2(MYH11):c.4920G>A (p.Arg1640=) rs199638486
NM_002474.2(MYH11):c.5076A>G (p.Leu1692=) rs1555551468
NM_002474.2(MYH11):c.5160C>T (p.Ser1720=) rs199564260
NM_002474.2(MYH11):c.5511A>G (p.Lys1837=) rs111697558
NM_002474.2(MYH11):c.5529G>A (p.Ser1843=) rs146024732
NM_002474.2(MYH11):c.5566C>T (p.Leu1856=) rs142639688
NM_002474.2(MYH11):c.5595C>T (p.Ala1865=) rs760286479
NM_002474.2(MYH11):c.5652G>A (p.Arg1884=) rs150860193
NM_002474.2(MYH11):c.5691C>T (p.Asn1897=) rs149566621
NM_002474.2(MYH11):c.5733G>A (p.Thr1911=) rs372173243
NM_002474.2(MYH11):c.5742C>T (p.Asn1914=) rs146391904
NM_002474.2(MYH11):c.5796C>T (p.Asn1932=) rs149529195
NM_002474.2(MYH11):c.5800A>T (p.Thr1934Ser) rs113667224
NM_002474.2(MYH11):c.5829A>G (p.Gly1943=) rs199752132
NM_002474.2(MYH11):c.5874G>A (p.Thr1958=) rs761000142
NM_002474.2(MYH11):c.5886C>T (p.Asp1962=) rs140789717

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