ClinVar Miner

Submissions for variant NM_001193315.2(VIPAS39):c.1221C>T (p.Phe407=)

gnomAD frequency: 0.00001  dbSNP: rs886044709
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000354102 SCV000345994 uncertain significance not provided 2016-09-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000354102 SCV005827780 likely benign not provided 2025-02-01 criteria provided, single submitter clinical testing

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