Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10013495 1.000 0.040 4 144584486 intron variant C/T snv 0.23 1
rs10491678 1.000 0.040 9 29568688 intergenic variant T/A;C snv 1
rs10760580 1.000 0.040 9 98899368 TF binding site variant G/A snv 0.22 1
rs1080879 1.000 0.040 5 15054693 intergenic variant T/C;G snv 1
rs10928927 1.000 0.040 2 129710793 intergenic variant C/T snv 0.70 1
rs10929386 1.000 0.040 2 15766055 intergenic variant C/G;T snv 1
rs11046966 1.000 0.040 12 23524758 downstream gene variant T/C snv 0.24 1
rs111720447 1.000 0.040 7 69238318 intron variant C/A;T snv 1
rs11234554 1.000 0.040 11 86138052 intergenic variant C/A;G snv 1
rs11245387 1.000 0.040 10 124849256 intergenic variant C/G;T snv 1
rs114216682 1.000 0.040 1 53405413 intergenic variant G/A;C snv 1
rs11655567 1.000 0.040 17 71220546 intergenic variant T/C snv 0.40 1
rs12926803 1.000 0.040 16 58063696 regulatory region variant G/A;C snv 1
rs12956045 1.000 0.040 18 13843247 intergenic variant A/G;T snv 1
rs13408379 1.000 0.040 2 129715649 intergenic variant G/A snv 0.21 1
rs139218005 1.000 0.040 8 53535172 upstream gene variant A/G snv 1.5E-02 1
rs140706189 1.000 0.040 14 60684707 intergenic variant T/G snv 1.5E-02 1
rs1412076 1.000 0.040 9 132157503 upstream gene variant A/G snv 0.47 1
rs143376495 1.000 0.040 6 50885046 intergenic variant T/C;G snv 1
rs147388556 1.000 0.040 1 82605935 intron variant T/C snv 1.2E-02 1
rs16906714 1.000 0.040 12 30707623 downstream gene variant T/C snv 4.9E-02 1
rs17404727 1.000 0.040 15 49711886 intergenic variant T/C snv 0.25 1
rs17634369 1.000 0.040 7 50281878 intergenic variant G/A snv 0.49 1
rs17759204 1.000 0.040 3 55124197 intergenic variant A/G snv 0.21 1
rs188637550 1.000 0.040 8 17825558 intron variant T/C snv 4.3E-03 1