ClinVar Miner

Submissions for variant NM_025216.3(WNT10A):c.420C>T (p.Gly140=)

gnomAD frequency: 0.00003  dbSNP: rs148979463
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000330331 SCV000427538 likely benign SchC6pf-Schulz-Passarge syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000389567 SCV000427539 likely benign Selective tooth agenesis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000295107 SCV000427540 likely benign Odonto-onycho-dermal dysplasia 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001447441 SCV001650506 likely benign Odonto-onycho-dermal dysplasia; Tooth agenesis, selective, 4 2024-01-31 criteria provided, single submitter clinical testing

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