ClinVar Miner

Submissions for variant NM_014000.2(VCL):c.1192C>T (p.Pro398Ser) (rs201528612)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biesecker Lab/Clinical Genomics Section,National Institutes of Health RCV000172500 SCV000054748 uncertain significance not provided 2013-06-24 criteria provided, single submitter research
Fulgent Genetics,Fulgent Genetics RCV000763670 SCV000894550 uncertain significance Dilated cardiomyopathy 1W; Familial hypertrophic cardiomyopathy 15 2018-10-31 criteria provided, single submitter clinical testing

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