ClinVar Miner

Submissions for variant NM_139281.3(WDR36):c.1717-20T>A

gnomAD frequency: 0.10369  dbSNP: rs59359951
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
GeneDx RCV001609624 SCV001841761 benign not provided 2019-09-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001609624 SCV002374977 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501972 SCV002809325 likely benign Glaucoma 1, open angle, G 2022-04-11 criteria provided, single submitter clinical testing

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