ClinVar Miner

Submissions for variant NM_025216.3(WNT10A):c.660C>T (p.Phe220=)

gnomAD frequency: 0.00002  dbSNP: rs765046353
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000872013 SCV001013759 likely benign Odonto-onycho-dermal dysplasia; Tooth agenesis, selective, 4 2024-09-28 criteria provided, single submitter clinical testing
Natera, Inc. RCV001271494 SCV001452693 uncertain significance SchC6pf-Schulz-Passarge syndrome 2020-01-24 no assertion criteria provided clinical testing

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