ClinVar Miner

Submissions for variant NM_025216.3(WNT10A):c.902G>C (p.Arg301Pro)

gnomAD frequency: 0.00002  dbSNP: rs777460453
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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 RCV001443172 SCV001646140 likely benign Odonto-onycho-dermal dysplasia; Tooth agenesis, selective, 4 2023-09-21 criteria provided, single submitter clinical testing

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