ClinVar Miner

List of variants reported as uncertain significance for pancreas disorder by Molecular Genetics, Madras Diabetes Research Foundation

Included ClinVar conditions (165):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_000525.4(KCNJ11):c.1084G>A (p.Ala362Thr) rs755839409 0.00001
NM_000545.8(HNF1A):c.340C>T (p.Arg114Cys) rs774996577 0.00001
NM_000545.8(HNF1A):c.901G>A (p.Ala301Thr) rs555681479 0.00001
NM_000352.6(ABCC8):c.208G>C (p.Gly70Arg) rs764349043
NM_000352.6(ABCC8):c.2539G>A (p.Ala847Thr) rs561593131
NM_000352.6(ABCC8):c.2912A>T (p.Glu971Val) rs1431503235
NM_000352.6(ABCC8):c.2974C>T (p.Arg992Cys) rs1954577653
NM_000352.6(ABCC8):c.4361T>G (p.Leu1454Arg) rs2133398519
NM_000458.4(HNF1B):c.961A>G (p.Asn321Asp) rs1208894321
NM_000545.8(HNF1A):c.733G>A (p.Gly245Arg) rs2135841196

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