ClinVar Miner

Submissions for variant NM_006005.3(WFS1):c.1752G>A (p.Gln584=)

gnomAD frequency: 0.00011  dbSNP: rs76577786
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002206694 SCV002368806 likely benign not provided 2024-05-13 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002507909 SCV002807843 likely benign Cataract 41; Wolfram syndrome 1; Autosomal dominant nonsyndromic hearing loss 6; Type 2 diabetes mellitus; Wolfram-like syndrome 2022-02-03 criteria provided, single submitter clinical testing

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