rs1064793998, 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.
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
108 0.882 0.080 7 44153325 missense variant C/T snv 0.720 1.000 8 1998 2016
Diabetes mellitus autosomal dominant type II (disorder)
139 0.882 0.080 7 44153325 missense variant C/T snv 0.700 1.000 8 1998 2016
Maturity onset diabetes mellitus in young
49 0.882 0.080 7 44153325 missense variant C/T snv 0.010 1.000 1 2005 2005