ClinVar Miner

Submissions for variant NM_000102.4(CYP17A1):c.654C>T (p.Val218=)

gnomAD frequency: 0.00002  dbSNP: rs375350911
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001440871 SCV001643787 likely benign not provided 2024-01-28 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002495616 SCV002799180 likely benign Deficiency of steroid 17-alpha-monooxygenase 2021-09-27 criteria provided, single submitter clinical testing

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