Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 15
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 15
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs12365699 0.882 0.120 11 118872577 regulatory region variant G/A snv 0.12 5
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 5
rs55646091 0.925 0.080 11 76588387 upstream gene variant G/A snv 3.0E-02 5
rs9687958 0.827 0.120 5 40496321 intron variant G/T snv 0.60 5
rs10414065 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 4
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 4
rs1438673 0.882 0.120 5 111131801 downstream gene variant C/T snv 0.61 4
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 4
rs2025758 0.882 0.160 10 8799706 intergenic variant T/C snv 0.41 4
rs6594499 0.882 0.120 5 111134439 downstream gene variant C/A snv 0.56 4
rs1102705 0.925 0.080 1 172731728 intergenic variant G/A snv 0.93 3
rs2381416 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 3
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 3
rs3853750 0.882 0.160 5 110818610 intergenic variant T/C snv 0.30 3
rs6461503 0.925 0.080 7 20521373 intergenic variant T/C;G snv 3
rs6489785 1.000 0.040 12 120925921 TF binding site variant T/C snv 0.68 3
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 3