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
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
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
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 6
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 5
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs12365699 0.882 0.120 11 118872577 regulatory region variant G/A snv 0.12 5
rs1444782 0.851 0.240 10 9016708 intergenic variant G/A snv 0.35 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
rs7936312 0.882 0.080 11 76582682 intergenic variant G/T snv 0.44 5
rs10414065 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 4
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 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
rs148696809 0.851 0.160 6 28966575 downstream gene variant T/C snv 5.3E-02 4
rs17144046 0.882 0.120 10 8564051 intergenic variant A/G snv 0.28 4
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 4