rs193922283, GCK

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Diabetes mellitus autosomal dominant type II (disorder)
CUI: C0342277
Disease: Diabetes mellitus autosomal dominant type II (disorder)
139 0.851 0.080 7 44145176 missense variant G/A snv 0.700 0
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.851 0.080 7 44145176 missense variant G/A snv 0.700 0
DIABETES MELLITUS, PERMANENT NEONATAL
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
108 0.851 0.080 7 44145176 missense variant G/A snv 0.700 0
Hyperinsulinemic hypoglycemia, familial, 3
CUI: C1865290
Disease: Hyperinsulinemic hypoglycemia, familial, 3
11 0.851 0.080 7 44145176 missense variant G/A snv 0.700 0