ClinVar Miner

List of variants reported as benign for cardiomyopathy by Blueprint Genetics

Included ClinVar conditions (522):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_002471.4(MYH6):c.1763A>C (p.Asp588Ala) rs142992009 0.00153
NM_001005242.3(PKP2):c.1114G>C (p.Ala372Pro) rs200586695
NM_024422.6(DSC2):c.2686_2687dup (p.Ala897fs) rs200056085

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