Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 10
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 7
rs10978777 1.000 0.080 9 107268309 intergenic variant G/A;C snv 2
rs114031744 1.000 0.080 10 123610085 intergenic variant A/G snv 1.7E-02 2
rs11509197 1.000 0.080 7 118641356 intergenic variant C/T snv 0.38 2
rs117854110 1.000 0.080 7 105603002 upstream gene variant C/A;T snv 2
rs13175840 1.000 0.080 5 133861647 regulatory region variant A/G snv 0.25 2
rs1481805 1.000 0.080 8 71121190 intron variant A/T snv 0.58 2
rs16850360 4 74006728 intron variant A/G snv 4.2E-02 2
rs6506897 1.000 0.080 18 31215320 intergenic variant G/A snv 0.62 2
rs712964 22 19168604 upstream gene variant T/C snv 0.66 2
rs73169578 1.000 0.080 13 21120420 intergenic variant G/A snv 3.1E-02 2
rs74155456 1.000 0.080 10 61070020 intergenic variant T/C snv 2.3E-02 2
rs74910095 1.000 0.080 5 63545132 intergenic variant T/A snv 3.7E-02 2
rs76294234 1.000 0.080 4 83241025 intron variant A/G snv 1.5E-02 2
rs7689240 1.000 0.080 4 35313869 intergenic variant A/G snv 0.21 2
rs77934287 1.000 0.080 12 23071319 intron variant A/G;T snv 2
rs9641609 1.000 0.080 7 118657790 regulatory region variant A/G snv 0.38 2
rs10502575 18 31756628 downstream gene variant A/G snv 6.9E-02 1
rs12507628 4 72779634 regulatory region variant G/A snv 0.13 1
rs1851024 4 71842104 intergenic variant G/A snv 0.93 1
rs1998013 1 55492357 intron variant C/T snv 4.4E-03 1
rs2168889 4 74357994 intergenic variant A/G snv 4.7E-02 1
rs616082 18 31787677 intergenic variant C/A;T snv 1