Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
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
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
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 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
rs6594499 0.882 0.120 5 111134439 downstream gene variant C/A snv 0.56 4
rs10036789 1.000 0.080 5 72400091 regulatory region variant C/A;G snv 3
rs1102705 0.925 0.080 1 172731728 intergenic variant G/A snv 0.93 3
rs13277355 0.882 0.120 8 127765473 intergenic variant A/G snv 0.71 3
rs1775554 0.882 0.080 10 9012377 intergenic variant A/C snv 0.35 3
rs4739738 0.882 0.120 8 80379410 intron variant G/A snv 0.60 3
rs6461503 0.925 0.080 7 20521373 intergenic variant T/C;G snv 3
rs7734635 0.925 0.080 5 110823145 intergenic variant A/G snv 0.30 3
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 3
rs10158467 0.925 0.080 1 173162354 regulatory region variant A/G;T snv 2
rs10187276 0.925 0.080 2 227805721 upstream gene variant T/C snv 0.62 2