Source: GWASDB ×
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 25
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 7
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 3
rs853789
ABCB11
2 168944978 intron variant A/G;T snv 0.75 3
rs2877716
ADCY5
3 123375604 intron variant T/C snv 0.76 3
rs5015480 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 2
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 2
rs927332 6 6331640 intergenic variant T/C snv 0.48 1
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 1
rs12243326
TCF7L2
0.925 0.160 10 113029056 intron variant T/C snv 0.27 1
rs17271305
VPS13C
15 62040781 intron variant A/G;T snv 1