ClinVar Miner

Submissions for variant NM_000102.4(CYP17A1):c.318C>T (p.Ser106=)

gnomAD frequency: 0.00001  dbSNP: rs766679884
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002169781 SCV002337367 likely benign not provided 2023-08-10 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002498126 SCV002805046 likely benign Deficiency of steroid 17-alpha-monooxygenase 2021-07-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002169781 SCV005220119 likely benign not provided criteria provided, single submitter not provided

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