ClinVar Miner

Submissions for variant NM_000102.4(CYP17A1):c.276C>T (p.Asp92=)

gnomAD frequency: 0.00002  dbSNP: rs535575638
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 RCV000928257 SCV001073864 likely benign not provided 2024-06-03 criteria provided, single submitter clinical testing
Natera, Inc. RCV001832101 SCV002093633 likely benign Deficiency of steroid 17-alpha-monooxygenase 2020-02-25 no assertion criteria provided clinical testing

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