Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2064009 8 115995625 intron variant C/G;T snv 1
rs6987444 8 116064090 intron variant G/A snv 0.68 1
rs6901250 6 116792862 synonymous variant G/A snv 0.33 0.29 1
rs1736060 8 11807229 intron variant C/G;T snv 0.54 1
rs1616534 8 11808942 intron variant C/G;T snv 9.8E-06; 0.58 1
rs10435719 8 11919395 downstream gene variant C/T snv 0.48 2
rs2686555 12 120657369 intron variant A/G snv 0.52 2
rs4871137 8 120856311 intergenic variant G/T snv 0.55 2
rs2650000 0.851 0.200 12 120951159 intron variant A/C snv 0.70 2
rs7305618 0.925 0.160 12 120965129 intron variant C/T snv 0.28 2
rs7953249 0.882 0.160 12 120965921 splice region variant G/A snv 0.59 4
rs2251468 12 120967323 intron variant C/A;G;T snv 1
rs1169288 0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 8
rs2244608 0.882 0.160 12 120979185 intron variant A/G snv 0.29 6
rs1169286 1.000 0.080 12 120981253 intron variant T/C snv 0.39 1
rs1169284 12 120982123 intron variant T/C snv 0.32 1
rs7979473 12 120982457 intron variant A/C;G snv 2
rs7979478 12 120982460 intron variant A/C;G;T snv 1
rs1183910 1.000 0.080 12 120983004 intron variant G/A snv 0.28 3
rs9738226 12 120985856 intron variant A/G snv 0.62 1
rs2393791 0.925 0.160 12 120986153 intron variant C/T snv 0.62 2
rs7310409 0.925 0.160 12 120987058 intron variant A/C;G;T snv 3
rs12427353 1.000 0.080 12 120989098 intron variant G/A;C;T snv 1
rs2259816 0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40 2
rs1169310 12 121001630 3 prime UTR variant G/A snv 0.31 1