ClinVar Miner

Submissions for variant NM_001193315.2(VIPAS39):c.861C>T (p.Ser287=)

gnomAD frequency: 0.00275  dbSNP: rs148698913
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000174793 SCV000226161 benign not specified 2015-03-26 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV000174793 SCV000313891 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000973719 SCV001121488 benign not provided 2024-01-21 criteria provided, single submitter clinical testing
GeneDx RCV000973719 SCV001782461 likely benign not provided 2021-04-20 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000973719 SCV005217792 likely benign not provided criteria provided, single submitter not provided

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