Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10078021 5 75742606 intergenic variant T/G snv 0.51 1
rs10103353 8 81937217 intergenic variant C/T snv 0.35 1
rs1015291 12 19831845 intron variant A/G snv 0.55 1
rs10184839 2 181081388 intron variant A/T snv 0.77 1
rs1040922 20 10787163 intron variant G/T snv 0.27 1
rs10751962 10 4130519 intergenic variant C/G;T snv 1
rs1081707 2 96381261 downstream gene variant G/A snv 0.24 1
rs10822407 10 65024342 intergenic variant T/C snv 0.30 1
rs10864859 2 120682642 downstream gene variant G/C;T snv 1
rs1098708 12 27168179 intergenic variant A/G snv 0.35 1
rs11022734 11 13260033 intergenic variant A/G snv 0.64 1
rs111304266 5 57293715 intergenic variant C/G snv 2.7E-02 1
rs113134141 3 46820449 intergenic variant A/G snv 0.17 1
rs114503346 5 172765347 intron variant C/T snv 2.7E-02 1
rs115234772 2 53423157 TF binding site variant A/G snv 3.7E-03 1
rs115726563 6 31098642 intergenic variant C/T snv 1
rs11628933 14 60234185 intergenic variant G/C;T snv 1
rs11671323 19 21696775 intergenic variant A/G snv 0.41 1
rs11681462 2 42125427 intergenic variant A/C snv 0.15 1
rs117059939 14 36401137 intron variant G/T snv 9.5E-03 1
rs11780200 8 119446281 intron variant G/A snv 0.19 1
rs11923667 3 101549236 regulatory region variant T/A snv 0.40 1
rs11931572 4 30084482 intergenic variant A/C snv 1.6E-02 1
rs1220128 2 157643390 intergenic variant G/A;C snv 1
rs1240716 1 1410616 non coding transcript exon variant G/A;T snv 1