ClinVar Miner

Submissions for variant NM_025216.3(WNT10A):c.1092G>A (p.Lys364=)

dbSNP: rs1225945394
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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 RCV001479827 SCV001684133 likely benign Odonto-onycho-dermal dysplasia; Tooth agenesis, selective, 4 2023-08-25 criteria provided, single submitter clinical testing

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