ClinVar Miner

List of variants in gene MYH6 reported as likely benign for not provided

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Total variants: 21
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HGVS dbSNP
NM_002471.3(MYH6):c.1131C>T (p.Asp377=) rs61742472
NM_002471.3(MYH6):c.1485C>T (p.Phe495=) rs181613656
NM_002471.3(MYH6):c.1539C>T (p.Asp513=)
NM_002471.3(MYH6):c.1763A>C (p.Asp588Ala) rs142992009
NM_002471.3(MYH6):c.2206C>A (p.Gln736Lys) rs201411075
NM_002471.3(MYH6):c.2591C>T (p.Thr864Met) rs200153625
NM_002471.3(MYH6):c.3010G>T (p.Ala1004Ser) rs143978652
NM_002471.3(MYH6):c.3027G>A (p.Leu1009=)
NM_002471.3(MYH6):c.3199A>G (p.Ser1067Gly) rs145508517
NM_002471.3(MYH6):c.3303G>A (p.Val1101=) rs143825034
NM_002471.3(MYH6):c.3883G>C (p.Glu1295Gln) rs34935550
NM_002471.3(MYH6):c.4026C>T (p.Cys1342=) rs141062252
NM_002471.3(MYH6):c.4359+5A>G rs193283041
NM_002471.3(MYH6):c.4359+8A>C rs188675676
NM_002471.3(MYH6):c.4665C>T (p.His1555=)
NM_002471.3(MYH6):c.5403G>A (p.Glu1801=) rs762151922
NM_002471.3(MYH6):c.5476G>A (p.Gly1826Ser) rs202141059
NM_002471.3(MYH6):c.5477G>A (p.Gly1826Asp) rs200260229
NM_002471.3(MYH6):c.5514G>T (p.Ser1838=) rs727503232
NM_002471.3(MYH6):c.5642A>G (p.Lys1881Arg) rs750886219
NM_002471.3(MYH6):c.960C>T (p.Ser320=)

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