ClinVar Miner

List of variants reported as likely benign for Cardiomyopathy by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 12
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HGVS dbSNP gnomAD frequency
NM_007078.3(LDB3):c.690-4A>G rs45529531 0.00427
NM_001035.3(RYR2):c.10254C>T (p.Asn3418=) rs138073811 0.00264
NM_033337.3(CAV3):c.417C>T (p.Val139=) rs147250678 0.00043
NM_000335.5(SCN5A):c.5181C>T (p.Cys1727=) rs193922726 0.00011
NM_170707.4(LMNA):c.357-20C>T rs193922724 0.00004
NM_002471.4(MYH6):c.5508A>G (p.Ala1836=) rs193922654 0.00001
NM_000039.3(APOA1):c.162G>C (p.Val54=) rs193922099
NM_001079802.2(FKTN):c.1023G>A (p.Pro341=) rs146967918
NM_001103.4(ACTN2):c.2577C>T (p.Ala859=) rs193922636
NM_002471.4(MYH6):c.3979-8del rs193922652
NM_004415.4(DSP):c.6153C>G (p.Ala2051=) rs193922670
NM_024422.6(DSC2):c.942+16A>T rs111347888

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