Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13394720 1.000 2 233593475 intergenic variant T/C snv 7.0E-02 6
rs2741027 1.000 0.040 2 233609365 downstream gene variant G/A snv 0.22 4
rs17864661 2 233587096 downstream gene variant C/T snv 0.14 3
rs2602362 2 233607902 downstream gene variant A/C snv 0.22 3
rs2602363 2 233611879 intergenic variant T/C snv 0.22 3
rs2602364 2 233615583 upstream gene variant G/A snv 0.22 3
rs2741019 2 233602042 upstream gene variant C/A;G snv 3
rs2741021 2 233603237 upstream gene variant C/T snv 0.22 3
rs2741028 2 233610268 intergenic variant G/A;T snv 3
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