Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 6
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs6859
NECTIN2
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 6
rs1701704
LOC105369781 ; IKZF4
0.851 0.200 12 56018703 intron variant T/G snv 0.25 5
rs2927438 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 5
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 4
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 4
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 4
rs8106922
TOMM40
1.000 0.080 19 44898409 intron variant A/G snv 0.36 4
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 3
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 3
rs11755527
BACH2
0.851 0.360 6 90248512 intron variant C/G snv 0.36 3
rs12518099
LINC01339
0.925 0.120 5 90250292 intron variant A/G;T snv 3
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 3
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 3
rs4689388
WFS1
0.882 0.360 4 6268329 upstream gene variant G/A snv 0.64 3
rs4712523
CDKAL1
0.925 0.120 6 20657333 intron variant A/G snv 0.41 3
rs4788084
IL27
0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 3