ClinVar Miner

List of variants in gene MYH6 reported as uncertain significance by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Total variants: 10
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HGVS dbSNP
NM_002471.3(MYH6):c.2217T>C (p.Asp739=) rs374177807
NM_002471.3(MYH6):c.3010G>T (p.Ala1004Ser) rs143978652
NM_002471.3(MYH6):c.3327A>G (p.Lys1109=) rs755818414
NM_002471.3(MYH6):c.3437dup (p.Glu1147fs) rs397516761
NM_002471.3(MYH6):c.3672C>G (p.Ser1224Arg) rs755267212
NM_002471.3(MYH6):c.4905C>T (p.Asn1635=) rs143048583
NM_002471.3(MYH6):c.5393G>A (p.Arg1798Gln) rs759281871
NM_002471.3(MYH6):c.5400C>T (p.Asp1800=) rs144329079
NM_002471.3(MYH6):c.5491G>A (p.Glu1831Lys) rs367834703
NM_002471.3(MYH6):c.5652C>T (p.Ala1884=) rs200662317

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