Disease: Fasting blood glucose measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22