ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.2572A>C (p.Ser858Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Klaassen Lab,Charite University Medicine Berlin RCV000787296 SCV000926216 likely pathogenic Left ventricular noncompaction 10 no assertion criteria provided research Found in compound heterozygosity with arr[hg19] 11p11.2(47339995x2,47343435 _47375684x1,47387184x2)

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