ClinVar Miner

Submissions for variant NM_003392.7(WNT5A):c.417C>T (p.Tyr139=)

gnomAD frequency: 0.00030  dbSNP: rs371576999
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000596243 SCV000701686 uncertain significance not provided 2016-09-30 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000596243 SCV001153984 uncertain significance not provided 2017-08-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000596243 SCV001731703 benign not provided 2025-01-08 criteria provided, single submitter clinical testing

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