ClinVar Miner

Submissions for variant NM_001193315.2(VIPAS39):c.1014C>T (p.Phe338=)

gnomAD frequency: 0.00001  dbSNP: rs199839422
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000595619 SCV000706109 benign not specified 2017-02-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000895156 SCV001039181 benign not provided 2024-11-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000895156 SCV005295136 benign not provided criteria provided, single submitter not provided

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