rs1064794268, GCK

N. diseases: 2
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)
139 0.925 0.080 7 44153396 missense variant T/G snv 0.700 1.000 3 2000 2014
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
108 0.925 0.080 7 44153396 missense variant T/G snv 0.700 1.000 3 2000 2014