ClinVar Miner

Submissions for variant NM_006005.3(WFS1):c.876C>G (p.Pro292=)

dbSNP: rs1159812254
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001727283 SCV001962559 likely benign not provided 2021-07-01 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002496051 SCV002801974 likely benign Cataract 41; Wolfram syndrome 1; Autosomal dominant nonsyndromic hearing loss 6; Type 2 diabetes mellitus; Wolfram-like syndrome 2021-08-16 criteria provided, single submitter clinical testing

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