Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 15
rs10484761 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 7
rs12413624 0.851 0.120 10 118519432 intergenic variant T/A snv 0.34 5
rs31563 0.851 0.160 5 135899917 intron variant C/A;T snv 5
rs312986 0.925 0.080 18 1898710 intron variant A/G;T snv 3
rs1430055 2 16499521 intergenic variant G/A snv 0.61 2
rs6503659 1.000 0.040 17 41741012 intergenic variant A/C;G;T snv 2
rs6772209 1.000 0.080 3 175929377 intergenic variant G/A snv 4.1E-02 2
rs7578456 1.000 0.080 2 201370625 intergenic variant A/G snv 0.57 2
rs8030672 1.000 0.080 15 68766745 intergenic variant T/A snv 5.4E-02 2
rs10502995 18 55138645 regulatory region variant G/A snv 0.20 1
rs11972901 7 85966605 intergenic variant A/G snv 0.47 1
rs1453029 18 41000207 intergenic variant T/C snv 7.0E-02 1
rs1737076 6 29757544 intron variant A/G snv 0.45 1
rs17450420 13 104386796 intergenic variant A/G snv 5.9E-02 1
rs2378002 1 218749016 intergenic variant G/T snv 5.9E-02 1
rs2984526 9 72372344 intergenic variant C/G snv 0.48 1
rs4283388 2 172374994 downstream gene variant C/T snv 0.33 1
rs4503732 15 46350065 intron variant C/A;G;T snv 0.92 1
rs6023640 20 54842266 intergenic variant T/G snv 0.73 1
rs7206735 16 50114597 intron variant T/C snv 0.39 1
rs753544 6 29812752 upstream gene variant C/T snv 0.27 1
rs896570 10 47145727 intergenic variant C/T snv 0.50 1