ClinVar Miner

Submissions for variant NM_006005.3(WFS1):c.713-19G>A

dbSNP: rs776845938
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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 RCV002193499 SCV002486028 likely benign not provided 2022-10-17 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500392 SCV002812503 likely benign Cataract 41; Wolfram syndrome 1; Autosomal dominant nonsyndromic hearing loss 6; Type 2 diabetes mellitus; Wolfram-like syndrome 2021-11-19 criteria provided, single submitter clinical testing

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