Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1058319 1.000 0.040 20 63743036 3 prime UTR variant C/A;T snv 0.21 2
rs1059394 0.925 0.080 18 672792 3 prime UTR variant C/T snv 0.40 2
rs1059513 0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs1064794096 1.000 0.040 10 87864514 missense variant A/C;T snv 2
rs10764901 1.000 0.040 10 129716598 intron variant A/G snv 0.62 1
rs10842893 1.000 0.040 12 27269953 intron variant C/T snv 7.1E-02 1
rs10852606 0.882 0.040 16 50094961 intron variant T/A;C snv 4
rs10892258 0.925 0.120 11 118709156 intron variant G/A snv 0.19 4
rs10924303 1.000 0.040 1 245683732 intron variant C/T snv 0.15 2
rs10924690 1.000 0.040 1 246320481 intron variant G/A snv 0.20 2
rs11079041 0.882 0.040 17 42262061 intron variant T/A;C snv 0.36 4
rs11163687 1.000 0.040 1 83199436 intergenic variant A/G snv 9.6E-02 2
rs11166389 1.000 0.040 1 100000723 non coding transcript exon variant G/A snv 0.15 2
rs111696067 1.000 0.040 12 132799954 intron variant T/C snv 5.3E-04 2
rs11196067 0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs11196172 0.708 0.200 10 112967084 intron variant G/A snv 0.13 18
rs11216930 1.000 0.040 11 118618067 intron variant A/C snv 0.22 2
rs11216943 1.000 0.040 11 118685689 downstream gene variant G/A snv 0.20 1
rs11233250 0.882 0.040 11 82685972 intron variant C/T snv 0.11 4
rs1131239 1.000 0.040 4 121696590 5 prime UTR variant G/A;C;T snv 0.12 0.17 1
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11337 0.925 0.120 8 41510767 3 prime UTR variant T/G snv 0.93 4
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70