Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs6921438 0.776 0.360 6 43957870 intergenic variant G/A;C snv 10
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 6
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 6
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 5
rs4761234 12 69338325 TF binding site variant T/C snv 0.36 5
rs72802342 0.851 0.040 16 75200974 downstream gene variant C/A snv 6.2E-02 5
rs413141 19 6675978 downstream gene variant A/G snv 0.84 4
rs2535627 1.000 0.040 3 52811089 downstream gene variant T/A;C;G snv 3
rs4657825 1.000 0.040 1 196615191 intergenic variant A/G;T snv 3
rs7260330 19 44932959 downstream gene variant A/G snv 0.39 3
rs75627662 1.000 0.080 19 44910319 non coding transcript exon variant C/T snv 0.17 3
rs75759936 4 78698045 intergenic variant C/A snv 5.0E-03 3
rs759819 1.000 0.080 19 54304302 intron variant C/G;T snv 3
rs9296009 0.925 0.160 6 32146738 downstream gene variant A/T snv 0.21 3
rs10269783 7 49576607 intron variant G/A snv 0.36 2
rs10919543 1.000 0.080 1 161538827 intron variant A/G snv 0.28 2
rs11720167 3 165768357 intron variant T/A;G snv 2
rs11751347 6 160671406 intron variant C/T snv 6.2E-02 2
rs1456297 15 51672013 regulatory region variant C/A;G;T snv 2
rs182722517 19 50739310 TF binding site variant G/A snv 3.6E-03 2