ClinVar Miner

Submissions for variant NM_000216.4(ANOS1):c.98G>C (p.Arg33Pro)

gnomAD frequency: 0.00008  dbSNP: rs746075352
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002189698 SCV002346056 benign Hypogonadotropic hypogonadism 1 with or without anosmia 2025-01-06 criteria provided, single submitter clinical testing

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