rs193922289, 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.
Diabetes mellitus autosomal dominant type II (disorder)
139 0.882 0.080 7 44152420 missense variant C/T snv 4.0E-06 0.800 1.000 20 1992 2014
DIABETES MELLITUS, PERMANENT NEONATAL
108 0.882 0.080 7 44152420 missense variant C/T snv 4.0E-06 0.700 1.000 2 2001 2014
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
108 0.882 0.080 7 44152420 missense variant C/T snv 4.0E-06 0.010 1.000 1 2009 2009