ClinVar Miner

Submissions for variant NM_025216.3(WNT10A):c.775C>A (p.Arg259=)

gnomAD frequency: 0.00014  dbSNP: rs576855744
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001429167 SCV001631879 likely benign Odonto-onycho-dermal dysplasia; Tooth agenesis, selective, 4 2024-03-02 criteria provided, single submitter clinical testing
Natera, Inc. RCV001831485 SCV002078833 likely benign SchC6pf-Schulz-Passarge syndrome 2021-06-10 no assertion criteria provided clinical testing

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