ClinVar Miner

List of variants studied for Atrial fibrillation, familial, 18 by Invitae

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Total variants: 21
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HGVS dbSNP
NM_002476.2(MYL4):c.113C>A (p.Ala38Asp) rs780020430
NM_002476.2(MYL4):c.150C>T (p.Ala50=) rs143234546
NM_002476.2(MYL4):c.167T>C (p.Phe56Ser) rs144870368
NM_002476.2(MYL4):c.23C>T (p.Pro8Leu) rs957196759
NM_002476.2(MYL4):c.277G>A (p.Glu93Lys) rs369894969
NM_002476.2(MYL4):c.313+8C>A rs372826462
NM_002476.2(MYL4):c.314-4G>A rs114024716
NM_002476.2(MYL4):c.365A>G (p.His122Arg)
NM_002476.2(MYL4):c.405C>T (p.Phe135=) rs150593274
NM_002476.2(MYL4):c.406G>A (p.Val136Met) rs375241929
NM_002476.2(MYL4):c.418C>T (p.Arg140Cys) rs767035280
NM_002476.2(MYL4):c.419G>A (p.Arg140His) rs374127769
NM_002476.2(MYL4):c.446C>T (p.Thr149Met)
NM_002476.2(MYL4):c.487+1G>C rs769405762
NM_002476.2(MYL4):c.487+4T>C
NM_002476.2(MYL4):c.488-1G>A
NM_002476.2(MYL4):c.488-4G>A rs146859926
NM_002476.2(MYL4):c.488-5C>T rs376118927
NM_002476.2(MYL4):c.522G>A (p.Leu174=) rs767533462
NM_002476.2(MYL4):c.537G>A (p.Glu179=) rs181540609
NM_002476.2(MYL4):c.556A>T (p.Asn186Tyr) rs16941677

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