Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 6
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 5
rs3130350 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 5
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 5
rs2746150 0.851 0.240 6 29474924 downstream gene variant C/T snv 5.3E-02 4
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 4
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 4
rs1394371 0.925 0.080 15 78432127 intergenic variant C/T snv 0.22 3
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 3
rs3130893 0.882 0.160 6 29012930 intergenic variant A/G snv 5.3E-02 3
rs4887053 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 3
rs3132631 0.925 0.160 6 30376868 regulatory region variant C/T snv 0.11 2
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 2
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 2
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 1
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 5
rs11235604
ATG16L2
0.925 0.080 11 72822491 missense variant C/T snv 7.0E-03 2.3E-03 1
rs4808075
BABAM1 ; USHBP1
0.701 0.280 19 17279482 intron variant T/C snv 0.26 1
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 6
rs7216064
BPTF
1.000 0.040 17 67902693 intron variant G/A snv 0.22 1
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 2
rs558702
C2 ; ZBTB12 ; CYP21A2
0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 6
rs2151280
CDKN2B-AS1
0.701 0.360 9 22034720 non coding transcript exon variant G/A snv 0.46 3