Disease: Metabolic Syndrome X
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 4