ClinVar Miner

Submissions for variant NM_006005.3(WFS1):c.2565A>T (p.Ser855=)

dbSNP: rs1046316
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001721445 SCV000534439 likely benign not provided 2018-04-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001721445 SCV002381072 likely benign not provided 2024-11-30 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002502581 SCV002811930 likely benign Cataract 41; Wolfram syndrome 1; Autosomal dominant nonsyndromic hearing loss 6; Type 2 diabetes mellitus; Wolfram-like syndrome 2021-09-20 criteria provided, single submitter clinical testing

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