rs104894014, GCK

N. diseases: 3
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.
Hyperinsulinemic hypoglycemia, familial, 3
11 0.925 0.080 7 44145167 missense variant G/A snv 0.800 1.000 8 1998 2017
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.925 0.080 7 44145167 missense variant G/A snv 0.010 1.000 1 2002 2002
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.925 0.080 7 44145167 missense variant G/A snv 0.010 1.000 1 2002 2002