Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12985909 1.000 0.040 19 18328573 upstream gene variant C/T snv 0.51 1
rs13073817 1.000 0.040 3 18665366 intron variant G/A;C snv 1
rs13204742 1.000 0.040 6 127924620 intergenic variant G/T snv 9.3E-02 1
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 1
rs1373692 1.000 0.040 5 40431081 non coding transcript exon variant A/C;T snv 1
rs1487630 1.000 0.040 4 38334202 intergenic variant C/T snv 0.14 1
rs16967103 0.827 0.120 15 38606989 intergenic variant T/C snv 0.22 1
rs17234657 0.882 0.120 5 40401407 intergenic variant T/G snv 0.14 1
rs17694108 0.925 0.040 19 33240645 regulatory region variant G/A snv 0.22 1
rs1819333 1.000 0.040 6 166960059 upstream gene variant T/G snv 0.57 1
rs1819658 1.000 0.040 10 58153390 regulatory region variant C/G;T snv 1
rs1858074 1.000 0.040 5 132036306 intergenic variant A/G snv 0.22 1
rs194749 1.000 0.040 14 68807188 intergenic variant T/C snv 0.23 1
rs1992660 1.000 0.040 5 40414965 upstream gene variant C/T snv 0.58 1
rs1992662 1.000 0.040 5 40393750 intergenic variant A/G snv 0.29 1
rs2097432 1.000 0.040 6 32622994 TF binding site variant T/C snv 0.27 1
rs226534 1.000 0.040 X 127768516 intergenic variant A/G snv 0.34 1
rs247660 1.000 0.040 5 85462322 upstream gene variant A/C snv 0.21 1
rs255969 1.000 0.040 5 95314200 intergenic variant C/T snv 0.85 1
rs281379 1.000 0.040 19 48711017 downstream gene variant G/A snv 0.38 1
rs2858332 1.000 0.040 6 32713384 upstream gene variant G/T snv 0.54 1
rs3091315 1.000 0.040 17 34266646 upstream gene variant A/G snv 0.33 1
rs3091338 1.000 0.040 5 132067045 downstream gene variant C/T snv 0.30 1
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 1
rs359457 0.925 0.240 5 173852839 intergenic variant C/T snv 0.59 1