ClinVar Miner

Submissions for variant NM_025216.3(WNT10A):c.966G>C (p.Pro322=)

gnomAD frequency: 0.00002  dbSNP: rs767856988
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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 RCV001405080 SCV001606996 likely benign Odonto-onycho-dermal dysplasia; Tooth agenesis, selective, 4 2022-06-11 criteria provided, single submitter clinical testing
Natera, Inc. RCV001826205 SCV002078842 likely benign SchC6pf-Schulz-Passarge syndrome 2021-06-08 no assertion criteria provided clinical testing

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