rs750414160, KCNJ11

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.
Hyperinsulinemic hypoglycemia, familial, 2
50 0.925 0.120 11 17387224 missense variant C/A;T snv 4.0E-06; 2.0E-05 0.700 0
Congenital Hyperinsulinism
CUI: C3888018
Disease: Congenital Hyperinsulinism
27 0.925 0.120 11 17387224 missense variant C/A;T snv 4.0E-06; 2.0E-05 0.010 1.000 1 2011 2011