Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1877455 1.000 0.040 1 114556471 intergenic variant C/T snv 0.12 1
rs1895729 1.000 0.040 11 107113002 intergenic variant G/A snv 0.37 1
rs1896731 1.000 0.040 5 25898911 intergenic variant T/C snv 0.38 1
rs1936295 1.000 0.040 10 117902581 intergenic variant T/C snv 0.83 1
rs2779251 1.000 0.040 17 27804300 synonymous variant G/A snv 0.30 0.16 1
rs288604 1.000 0.040 16 62638708 intergenic variant G/A snv 0.87 1
rs289858 1.000 0.040 2 151195812 intergenic variant G/A snv 0.45 1
rs289932 1.000 0.040 2 151149511 intron variant C/T snv 0.39 1
rs29456 1.000 0.040 5 66244019 intergenic variant T/C snv 0.73 1
rs351871 1.000 0.040 5 77680214 regulatory region variant A/G;T snv 1
rs409649 1.000 0.040 5 25841054 intergenic variant A/G snv 0.29 1
rs4475231 1.000 0.040 5 25955208 regulatory region variant C/T snv 0.28 1
rs4701259 1.000 0.040 5 25900989 intergenic variant A/G snv 0.71 1
rs4701511 1.000 0.040 5 25895895 intergenic variant C/A snv 0.71 1
rs4925506 1.000 0.040 1 229676242 intergenic variant C/G;T snv 1
rs519700 1.000 0.040 13 88512065 intron variant T/A;C snv 1
rs6452304 1.000 0.040 5 25924119 intergenic variant T/C snv 0.69 1
rs6452305 1.000 0.040 5 25924513 intergenic variant A/C snv 0.69 1
rs6873221 1.000 0.040 5 25928457 intergenic variant G/A snv 0.47 1
rs6891206 1.000 0.040 5 25969270 intron variant T/C snv 0.65 1
rs6894102 1.000 0.040 5 25897447 intergenic variant T/C snv 0.38 1
rs7380139 1.000 0.040 5 25926257 intergenic variant A/G;T snv 1
rs7704909 1.000 0.040 5 25898812 intergenic variant T/A;C snv 1
rs7705715 1.000 0.040 5 25899305 intergenic variant T/C snv 0.71 1
rs7800565 1.000 0.040 7 16740384 TF binding site variant A/G snv 0.16 1