ClinVar Miner

Submissions for variant NM_025216.3(WNT10A):c.801G>A (p.Thr267=)

dbSNP: rs553058408
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000945611 SCV001091647 likely benign Odonto-onycho-dermal dysplasia; Tooth agenesis, selective, 4 2024-10-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004711438 SCV005258859 likely benign not provided criteria provided, single submitter not provided
Natera, Inc. RCV001277357 SCV001464302 uncertain significance SchC6pf-Schulz-Passarge syndrome 2020-10-24 no assertion criteria provided clinical testing

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