Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2047076 5 76762684 intergenic variant C/T snv 0.14 2
rs2485713 10 8423240 intron variant G/C;T snv 2
rs2521295 11 2327630 downstream gene variant T/A;C snv 2
rs2523552 6 31364177 upstream gene variant C/T snv 0.15 2
rs2732716 17 46245680 downstream gene variant T/A;C snv 2
rs2734037 3 128590041 intergenic variant C/T snv 0.34 2
rs2817441 6 156617565 regulatory region variant C/T snv 0.26 2
rs3095254 6 31253891 intergenic variant C/A;G snv 0.55 2
rs34018670 16 80809337 upstream gene variant -/AG delins 0.17 2
rs35110517 7 28267686 intergenic variant T/G snv 0.20 2
rs4020660 12 6402491 intergenic variant G/A;T snv 2
rs434216 16 85893407 regulatory region variant T/A;C snv 2
rs4385425 7 50267738 upstream gene variant A/G snv 0.40 2
rs4566648 4 83238066 intron variant T/G snv 0.47 2
rs4811020 20 50286497 downstream gene variant C/T snv 0.29 2
rs4843869 16 85941535 intron variant G/A snv 0.18 2
rs4919087 10 97312750 upstream gene variant A/G;T snv 2
rs531425523 22 17354388 upstream gene variant T/C snv 8.4E-05 2
rs55793580 9 124247116 regulatory region variant C/T snv 0.16 2
rs562398803 20 50492033 regulatory region variant AA/-;A;AAA;AAAA;AAAAA delins 2
rs58681483 17 59857293 downstream gene variant A/G snv 0.13 2
rs5875374 6 32459228 downstream gene variant -/AC delins 0.72 2
rs58904263 20 31813603 upstream gene variant -/G ins 2
rs62191825 2 219187607 downstream gene variant T/C snv 3.6E-02 2
rs62242983 3 46342431 intergenic variant T/A;C snv 0.14 2