ClinVar Miner

List of variants in gene MYH6 reported as uncertain significance by CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario

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Total variants: 27
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HGVS dbSNP
NM_002471.3(MYH6):c.1007C>G (p.Ala336Gly) rs138572790
NM_002471.3(MYH6):c.1449C>T (p.Asn483=) rs145447555
NM_002471.3(MYH6):c.2071G>A (p.Val691Ile) rs148915045
NM_002471.3(MYH6):c.2383C>T (p.Arg795Trp) rs202120238
NM_002471.3(MYH6):c.2538G>A (p.Glu846=) rs730880150
NM_002471.3(MYH6):c.2611C>T (p.Arg871Cys) rs376682837
NM_002471.3(MYH6):c.2612G>A (p.Arg871His) rs869025473
NM_002471.3(MYH6):c.2828G>A (p.Arg943His) rs766640013
NM_002471.3(MYH6):c.3010G>T (p.Ala1004Ser) rs143978652
NM_002471.3(MYH6):c.3177C>T (p.Gly1059=) rs529676901
NM_002471.3(MYH6):c.3303G>A (p.Val1101=) rs143825034
NM_002471.3(MYH6):c.3343-3delC rs1027186100
NM_002471.3(MYH6):c.3569C>T (p.Thr1190Ile) rs759117852
NM_002471.3(MYH6):c.3844C>G (p.Leu1282Val) rs1425090608
NM_002471.3(MYH6):c.3979-10C>A rs28730768
NM_002471.3(MYH6):c.3979-7_3979-4delTCCC rs745326238
NM_002471.3(MYH6):c.3979-7_3979-5delTCC rs397516764
NM_002471.3(MYH6):c.3979-8_3979-7delinsGC rs727503235
NM_002471.3(MYH6):c.4299C>T (p.Asp1433=) rs765006624
NM_002471.3(MYH6):c.4465G>A (p.Ala1489Thr) rs761539900
NM_002471.3(MYH6):c.5077G>A (p.Val1693Met) rs373457153
NM_002471.3(MYH6):c.5293G>A (p.Ala1765Thr) rs397516775
NM_002471.3(MYH6):c.5476_5477delinsAA (p.Gly1826Asn) rs878854502
NM_002471.3(MYH6):c.5748G>C (p.Glu1916Asp) rs1566503504
NM_002471.3(MYH6):c.643-5C>T rs199859986
NM_002471.3(MYH6):c.831G>T (p.Gln277His) rs140660481
NM_002471.3(MYH6):c.899-9C>T rs767945761

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