ClinVar Miner

Submissions for variant NM_006005.3(WFS1):c.315+17C>T

gnomAD frequency: 0.00006  dbSNP: rs766977344
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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 RCV002138970 SCV002469590 likely benign not provided 2023-12-18 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002505822 SCV002808163 likely benign Cataract 41; Wolfram syndrome 1; Autosomal dominant nonsyndromic hearing loss 6; Type 2 diabetes mellitus; Wolfram-like syndrome 2022-01-19 criteria provided, single submitter clinical testing

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