Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10164928 2 233893139 regulatory region variant C/T snv 5.8E-02 2
rs10175828 2 233473171 downstream gene variant G/C;T snv 2
rs10841642 12 20791740 intergenic variant C/A;T snv 2
rs10841645 12 20795800 intergenic variant A/C snv 0.59 2
rs10841648 12 20801623 intergenic variant C/A;T snv 2
rs11045505 12 20796512 intergenic variant C/T snv 0.59 2
rs1115381 2 233596639 intergenic variant T/C snv 0.71 2
rs11890203 2 233871485 upstream gene variant A/G snv 0.14 2
rs12313384 12 20790827 intergenic variant G/T snv 0.58 2
rs12549576 8 111963912 intergenic variant A/G snv 4.0E-02 2
rs12618259 2 233598275 intergenic variant A/T snv 0.22 2
rs12823467 12 20790642 intergenic variant T/C snv 0.59 2
rs13383300 2 233586823 downstream gene variant C/A;G snv 2
rs13387539 2 233573964 intergenic variant C/T snv 5.1E-02 2
rs13394291 2 233593094 intergenic variant T/C snv 8.8E-02 2
rs1551286 2 233606509 downstream gene variant C/G;T snv 2
rs17862835 2 233605867 downstream gene variant C/T snv 3.9E-02 2
rs17862836 2 233606117 downstream gene variant A/C snv 0.20 2
rs17862837 2 233608153 downstream gene variant T/A snv 0.33 2
rs17863756 2 233605334 downstream gene variant T/C snv 7.1E-02 2
rs17864662 2 233587888 downstream gene variant C/T snv 7.3E-02 2
rs17864666 2 233601211 upstream gene variant T/C snv 7.8E-02 2
rs17864668 2 233609776 intergenic variant T/G snv 0.15 2
rs17864669 2 233609868 intergenic variant T/C snv 4.4E-02 2
rs17868296 2 233588600 downstream gene variant A/G snv 4.9E-02 2