Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 10
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7
rs62106258 1.000 0.040 2 417167 upstream gene variant T/C snv 2.9E-02 5
rs1490384 6 126530014 intron variant C/G;T snv 4
rs900145 11 13272358 upstream gene variant C/T snv 0.62 4
rs1079866 0.925 0.080 7 41430495 intergenic variant C/G snv 0.13 3
rs13322435 3 157077679 upstream gene variant A/G snv 0.46 3
rs1659127 16 14294448 intergenic variant G/A;C;T snv 3
rs4549631 6 126645162 intron variant T/C;G snv 3
rs7821178 0.925 0.080 8 77181601 intergenic variant C/A;G;T snv 3
rs7846385 8 77247943 intergenic variant T/C snv 0.23 3
rs1172955 10 96117563 downstream gene variant T/A snv 0.60 2
rs13064915 3 137402401 intergenic variant T/C snv 0.42 2
rs3893384 1.000 0.040 15 79680713 regulatory region variant C/T snv 0.50 2
rs57149692 16 30130700 regulatory region variant G/C snv 0.46 2
rs6087709 20 35430145 upstream gene variant C/G snv 0.25 2
rs7141210 14 100716133 regulatory region variant T/C snv 0.55 2
rs7306275 12 49856328 upstream gene variant G/A snv 0.29 2
rs815715 3 61278410 intergenic variant C/G snv 0.54 2
rs9635759 17 51536424 regulatory region variant G/A snv 0.25 2
rs10094574 8 77203831 intergenic variant G/A;T snv 1
rs10150590 14 40456677 intergenic variant A/C snv 0.63 1