ClinVar Miner

Submissions for variant NM_000102.4(CYP17A1):c.315G>A (p.Ala105=)

dbSNP: rs150698224
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001404291 SCV001606189 likely benign not provided 2023-10-22 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002504676 SCV002802452 likely benign Deficiency of steroid 17-alpha-monooxygenase 2022-03-02 criteria provided, single submitter clinical testing

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