ClinVar Miner

Submissions for variant NM_025216.3(WNT10A):c.1146C>T (p.Asn382=)

dbSNP: rs759671927
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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 RCV001459699 SCV001663549 likely benign Odonto-onycho-dermal dysplasia; Tooth agenesis, selective, 4 2023-12-26 criteria provided, single submitter clinical testing
Natera, Inc. RCV001832599 SCV002078846 likely benign SchC6pf-Schulz-Passarge syndrome 2020-04-25 no assertion criteria provided clinical testing

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