Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10849023 12 4223312 intergenic variant C/T snv 0.22 4
rs11756659 6 25933704 upstream gene variant A/G;T snv 4
rs1569534 6 135130442 intergenic variant C/T snv 0.21 4
rs17064262 6 135144336 intergenic variant T/C snv 0.18 4
rs2050019 6 135142809 intergenic variant C/T snv 0.27 4
rs4916483 3 196180782 intergenic variant T/C snv 0.12 4
rs532591337 19 12459271 intron variant G/A snv 4.9E-05 4
rs643381 6 139518286 intron variant C/A;G snv 4
rs6538148 12 88424702 intergenic variant C/G;T snv 4
rs6569992 6 135131014 intergenic variant G/A;C;T snv 4
rs739385 7 93053295 regulatory region variant G/A;C snv 4
rs74929147 19 18302251 downstream gene variant G/A;C snv 4
rs932316 6 25640972 upstream gene variant T/C;G snv 4
rs9483788 6 135114363 intergenic variant T/C snv 0.19 4
rs10849020 12 4222843 intergenic variant C/G snv 0.22 3
rs11190134 10 99522443 upstream gene variant G/A snv 0.36 3
rs169219 6 25957164 intergenic variant C/A;G snv 3
rs17302154 2 196183605 intergenic variant A/C snv 9.8E-02 3
rs2537594 7 17774912 intergenic variant G/A snv 0.58 3
rs2869045 15 78426557 regulatory region variant T/C snv 0.78 3
rs34536858 19 35459272 intergenic variant A/G snv 0.33 3
rs35259020 9 134085798 intergenic variant CT/- delins 0.18 3
rs4332427 10 24569461 intergenic variant A/G snv 0.21 3
rs4675690 2 207643083 intergenic variant C/T snv 0.48 3
rs55771711 1.000 0.040 10 131989233 intergenic variant G/C snv 0.24 3