Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7907606 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 8
rs10425559 0.807 0.040 19 4837475 upstream gene variant A/G snv 0.66 7
rs10810657 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 7
rs231726 0.790 0.200 2 203876143 downstream gene variant C/T snv 0.36 7
rs7335046 0.807 0.040 13 99389484 downstream gene variant G/C snv 0.80 7
rs801114 0.827 0.120 1 228862088 downstream gene variant T/G snv 0.48 5
rs10424978 0.851 0.080 19 4837545 upstream gene variant C/A;G snv 4
rs1246946 0.851 0.040 6 4979722 downstream gene variant C/T snv 0.34 4
rs4761496 0.851 0.040 12 94733833 regulatory region variant T/A;C snv 0.23 4
rs59586681 0.851 0.040 20 2239664 intron variant A/G;T snv 0.34 4
rs6707137 0.882 0.040 2 88254832 regulatory region variant G/A snv 0.12 4
rs75790006 0.851 0.040 4 43211547 intron variant T/G snv 1.1E-02 4
rs10102591 0.882 0.040 8 80479448 intron variant G/T snv 0.28 3
rs11993814 0.882 0.040 8 80477556 intron variant C/T snv 0.39 3
rs12070203 0.882 0.040 1 228858641 downstream gene variant C/T snv 0.24 3
rs12205199 0.882 0.040 6 150032420 upstream gene variant C/A;T snv 3
rs12466910 0.882 0.040 2 11386590 downstream gene variant G/A;C;T snv 3
rs138501911 0.882 0.040 10 8920514 intergenic variant C/T snv 9.4E-02 3
rs17137933 0.882 0.040 7 17593140 intergenic variant C/T snv 0.21 3
rs209901 0.882 0.040 20 39117811 regulatory region variant T/A;C;G snv 3
rs34694416 0.882 0.040 6 32616594 regulatory region variant C/T snv 0.10 3
rs42905 0.882 0.040 5 68455394 regulatory region variant A/C snv 0.53 3
rs4710154 0.882 0.040 6 166981146 intron variant A/T snv 0.42 3
rs57244888 0.882 0.040 2 16280877 intron variant T/C snv 0.13 3
rs61824911 0.882 0.040 1 228843990 intergenic variant A/G snv 0.30 3