ClinVar Miner

Submissions for variant NM_025216.3(WNT10A):c.273C>A (p.Ile91=)

dbSNP: rs1011612159
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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 RCV001494793 SCV001699458 likely benign Odonto-onycho-dermal dysplasia; Tooth agenesis, selective, 4 2024-01-11 criteria provided, single submitter clinical testing

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