ClinVar Miner

Submissions for variant NM_004625.4(WNT7A):c.555C>T (p.Asn185=)

gnomAD frequency: 0.00170  dbSNP: rs149363953
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000597563 SCV000706602 uncertain significance not provided 2017-03-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000597563 SCV001116976 benign not provided 2022-06-12 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003935617 SCV004753919 likely benign WNT7A-related disorder 2019-10-11 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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