ClinVar Miner

Submissions for variant NM_000376.3(VDR):c.583+118A>T

gnomAD frequency: 0.03940  dbSNP: rs11574085
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001595557 SCV001829813 benign not provided 2018-10-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001595557 SCV005230640 benign not provided criteria provided, single submitter not provided

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