Disease: Diabetes
Source: GWASCAT ×
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 35
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 19
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 18
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 17
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 17
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 16
rs74617384
LPA
0.925 0.080 6 160576086 intron variant A/G;T snv 5