Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6696217 1 169491488 non coding transcript exon variant A/G snv 0.92 2
rs7659024 4 154599778 downstream gene variant G/A snv 0.26 2
rs970740 1 169510736 downstream gene variant C/T snv 0.95 2
rs10476160 5 175547573 regulatory region variant A/G;T snv 1
rs10746487 1 9278630 intergenic variant T/A;C snv 1
rs10919507 1 170885468 intron variant C/T snv 3.0E-02 1
rs113451833 8 64970119 downstream gene variant G/T snv 0.18 1
rs115063924 1 168741790 intron variant C/A;T snv 6.7E-03 1
rs12120558 1 170366687 downstream gene variant G/A snv 1.2E-02 1
rs12136148 1 170123530 intergenic variant T/G snv 6.9E-02 1
rs12450494 17 7304568 upstream gene variant T/A;C snv 1
rs12981279 19 10528857 intergenic variant T/C snv 0.41 1
rs142286129 11 54688761 upstream gene variant T/C snv 7.8E-03 1
rs1423386 5 62689026 intergenic variant A/G snv 0.19 1
rs143860577 11 50513762 intergenic variant A/T snv 7.3E-03 1
rs144405847 1 82342193 intron variant C/T snv 4.9E-02 1
rs147455989 11 50161397 intergenic variant T/C snv 7.8E-03 1
rs148268781 11 50663948 intergenic variant T/A;C snv 1
rs149903077 11 46328146 upstream gene variant G/T snv 9.5E-03 1
rs181813804 11 48706704 intergenic variant A/G snv 8.1E-03 1
rs182484222 11 48190205 intergenic variant G/A snv 7.7E-03 1
rs182879407 11 47199227 intergenic variant C/G;T snv 1
rs189484085 11 48511937 upstream gene variant C/T snv 8.1E-03 1
rs190666382 11 54553509 intergenic variant C/A;T snv 1
rs1910358 5 23907464 intergenic variant C/T snv 0.72 1