ClinVar Miner

Submissions for variant NM_000207.3(INS):c.94G>C (p.Gly32Arg)

dbSNP: rs80356664
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneReviews RCV000020213 SCV000040550 not provided Permanent neonatal diabetes mellitus no assertion provided literature only
UniProtKB/Swiss-Prot RCV000020213 SCV000091168 not provided Permanent neonatal diabetes mellitus no assertion provided not provided

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