Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11004733 0.882 0.040 10 55089584 intron variant C/T snv 2.9E-02 4
rs141252918 0.882 0.040 6 151506923 intron variant G/A;C snv 4
rs149268645 0.882 0.040 2 202968295 intron variant G/A snv 8.4E-02 4
rs4870888 0.882 0.040 8 124096736 intron variant T/C snv 0.39 4
rs62173322 0.882 0.040 2 169754519 intron variant A/G snv 0.32 4
rs76371172 0.882 0.040 15 31522252 intron variant T/G snv 9.1E-03 4
rs9577511 0.882 0.040 13 113337508 intron variant A/G snv 0.15 4
rs17173608 0.807 0.240 7 150339575 intron variant T/G snv 0.11 3
rs17387100 0.925 0.040 4 15993502 intron variant A/G snv 7.5E-02 3
rs111326206 1.000 0.040 3 142719589 intron variant T/C snv 7.9E-02 2
rs111367251 1.000 0.040 7 145271196 downstream gene variant C/G snv 7.8E-03 2
rs111625585 1.000 0.040 14 82337988 intergenic variant C/T snv 4.2E-02 2
rs113330417 1.000 0.040 14 66782703 intron variant A/G snv 1.6E-02 2
rs113386487 1.000 0.040 10 13316583 downstream gene variant A/G;T snv 2
rs116428372 1.000 0.040 16 539359 non coding transcript exon variant G/A snv 5.5E-02 2
rs13137453 1.000 0.040 4 152986727 intergenic variant A/G snv 1.9E-02 2
rs145440507 1.000 0.040 4 187479383 regulatory region variant A/T snv 7.8E-03 2
rs183414028 1.000 0.040 1 39976354 intergenic variant T/C snv 1.4E-05 2
rs184924771 1.000 0.040 11 25863658 intergenic variant A/C snv 1.2E-02 2
rs186736781 1.000 0.040 2 239551396 intergenic variant C/T snv 6.9E-03 2
rs191852465 1.000 0.040 7 63703764 downstream gene variant T/C snv 2
rs45593736 1.000 0.040 10 18666008 intron variant G/A snv 1.3E-02 2
rs62460873 1.000 0.040 7 85348650 intergenic variant T/C;G snv 7.8E-03 2
rs76347430 1.000 0.040 1 14069324 intron variant A/G snv 8.6E-03 2
rs77033326 1.000 0.040 4 88856467 intron variant G/A snv 1.3E-02 2