ClinVar Miner

Submissions for variant NM_000458.4(HNF1B):c.961A>G (p.Asn321Asp)

dbSNP: rs1208894321
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics, Madras Diabetes Research Foundation RCV002052016 SCV002318389 uncertain significance Maturity onset diabetes mellitus in young criteria provided, single submitter clinical testing

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