ClinVar Miner

Submissions for variant NM_000376.3(VDR):c.182C>T (p.Pro61Leu)

dbSNP: rs1945703092
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001235486 SCV001408175 uncertain significance not provided 2021-08-28 criteria provided, single submitter clinical testing

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