Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4518581 7 118970601 intergenic variant G/A snv 0.86 1
rs4665985 2 27531011 intergenic variant A/C;G snv 1
rs4730908 7 119017956 intergenic variant C/G;T snv 1
rs483916 8 9936091 intergenic variant A/C snv 0.51 1
rs4854723 3 133535414 regulatory region variant A/C snv 0.52 1
rs4854727 3 133539041 downstream gene variant A/G snv 0.65 1
rs4854733 3 133568221 intergenic variant A/G;T snv 1
rs4953404 2 46659003 intergenic variant G/A snv 0.69 1
rs6466686 7 118996763 intergenic variant C/T snv 0.58 1
rs6668659 1 11862241 upstream gene variant T/G snv 0.34 1
rs6763627 3 133543723 upstream gene variant C/G;T snv 1
rs6778062 3 133548309 upstream gene variant G/C snv 0.66 1
rs6785365 3 133543601 upstream gene variant A/G snv 0.65 1
rs6983393 8 119434109 intron variant T/A snv 0.34 1
rs6995407 8 8527137 regulatory region variant C/A;G snv 1
rs7614812 3 133545407 upstream gene variant C/A snv 0.62 1
rs7686419 4 39404750 upstream gene variant G/A;C snv 1
rs7733331 5 32828740 intergenic variant T/A;C snv 1
rs7812233 7 118978108 intergenic variant G/A snv 0.86 1
rs794905 3 41993238 intergenic variant C/G;T snv 1
rs79505281 8 35841899 intergenic variant C/A snv 1.7E-03 1
rs855350 1 63661333 downstream gene variant C/T snv 0.43 1
rs872134 3 133546688 upstream gene variant G/T snv 0.57 1
rs4936098 11 130410772 intron variant A/G;T snv 1
rs72640211 1 11778705 synonymous variant G/A snv 4.4E-02 4.8E-02 1