ClinVar Miner

Submissions for variant NM_025216.3(WNT10A):c.757-6C>T

dbSNP: rs757483068
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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 RCV001488623 SCV001693146 likely benign Odonto-onycho-dermal dysplasia; Tooth agenesis, selective, 4 2022-05-31 criteria provided, single submitter clinical testing

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