Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 8
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 7
rs7681423 4 154621096 intergenic variant C/T snv 0.26 5
rs1016988 5 132408882 upstream gene variant T/C snv 0.20 4
rs10034922 4 154599476 downstream gene variant G/A snv 5.2E-02 3
rs10226084 7 17957989 upstream gene variant T/C snv 0.46 3
rs12511469 4 154530607 downstream gene variant T/A snv 0.18 3
rs17690122 5 132532143 intron variant A/G;T snv 3
rs1938492 1 65652146 intergenic variant A/C snv 0.43 3
rs2710804 7 36044919 intron variant T/C snv 0.29 3
rs434943 14 68847342 intergenic variant G/A snv 0.27 3
rs4463047 4 154574381 downstream gene variant T/C snv 0.15 3
rs4508864 4 154560137 upstream gene variant C/G;T snv 3
rs4817986 21 39093586 regulatory region variant G/T snv 0.22 3
rs511154 3 136232079 intergenic variant A/G;T snv 3
rs6010044 22 50663510 intergenic variant A/C snv 0.20 3
rs743562 5 132536691 intron variant C/T snv 0.35 3
rs7673587 4 154559282 upstream gene variant C/T snv 0.24 3
rs2801231 1.000 0.080 X 122083259 intergenic variant T/A;C;G snv 2
rs7012814 8 9315848 intron variant G/A;T snv 2
rs7873907 9 89610568 downstream gene variant T/C snv 0.48 2
rs12699921 7 17954871 intergenic variant G/A snv 0.40 1
rs194714 14 68828731 intergenic variant T/C snv 0.24 1
rs194741 14 68821715 intergenic variant A/G snv 0.24 1
rs2376015 1 65658091 intergenic variant A/G snv 0.43 1