Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4898521 12 49361379 downstream gene variant T/A snv 0.97 2
rs2366858 7 80711306 regulatory region variant C/A snv 0.94 1
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 3
rs7483863
ZPR1
11 116781775 intron variant A/G snv 0.93 1
rs7350481 0.882 0.040 11 116715567 regulatory region variant T/C snv 0.93 3
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 6
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 1
rs2160669
ZPR1
1.000 0.040 11 116776891 3 prime UTR variant C/T snv 0.92 3
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 4
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 10
rs7298909
SBNO1
12 123346392 intron variant C/T snv 0.89 2
rs1215112
TTC39B
9 15303585 intron variant G/A snv 0.89 2
rs643531
TTC39B
9 15296036 intron variant C/A snv 0.89 1
rs686030
TTC39B
9 15304784 intron variant C/A snv 0.88 2
rs1461729
LOC157273
1.000 8 9329732 intron variant A/G snv 0.88 3
rs6601299
LOC157273
0.925 0.040 8 9327181 intron variant T/C snv 0.88 3
rs7239867
LOC105372112
18 49638347 TF binding site variant A/G snv 0.88 2
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs4240624
LOC157273
0.882 0.040 8 9326721 intron variant G/A snv 0.87 2
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87 6
rs2845885
FLRT1 ; MACROD1
11 64101590 intron variant C/T snv 0.87 5
rs471364
TTC39B
1.000 0.040 9 15289580 intron variant C/T snv 0.87 1