ClinVar Miner

Submissions for variant NM_025216.3(WNT10A):c.474C>T (p.Gly158=)

dbSNP: rs1944627971
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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 RCV002089634 SCV002330022 likely benign Odonto-onycho-dermal dysplasia; Tooth agenesis, selective, 4 2021-07-25 criteria provided, single submitter clinical testing

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