rs59852838, ABCC8

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 0.120 11 17453228 missense variant T/C snv 4.0E-05 4.9E-05 0.010 1.000 1 2008 2008
Impaired insulin secretion
CUI: C0948379
Disease: Impaired insulin secretion
14 0.882 0.120 11 17453228 missense variant T/C snv 4.0E-05 4.9E-05 0.010 1.000 1 2008 2008
Neonatal diabetes mellitus
CUI: C0158981
Disease: Neonatal diabetes mellitus
33 0.882 0.120 11 17453228 missense variant T/C snv 4.0E-05 4.9E-05 0.010 1.000 1 2008 2008