Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10152518 0.790 0.080 15 67884824 intergenic variant G/A;T snv 9
rs1035209 0.790 0.080 10 99585609 intergenic variant C/T snv 0.15 9
rs10849438 0.790 0.080 12 6302870 intergenic variant T/G snv 1.0E-01 9
rs10951878 0.790 0.080 7 46887097 downstream gene variant C/A;T snv 9
rs11169572 0.790 0.080 12 50823107 downstream gene variant T/C snv 0.42 9
rs11903757 0.763 0.160 2 191722478 intron variant T/C snv 0.16 9
rs11927424 0.790 0.080 3 88708681 intergenic variant A/G snv 0.39 9
rs12635946 0.790 0.080 3 113198071 intergenic variant C/T snv 0.32 9
rs12659017 0.790 0.080 5 126652483 intergenic variant G/A snv 0.27 9
rs13130787 0.790 0.080 4 93965880 intergenic variant T/C snv 0.35 9
rs13170463 0.790 0.080 5 7983139 downstream gene variant G/A;T snv 3.8E-02 9
rs1321310 0.790 0.080 6 36655347 regulatory region variant T/C snv 0.29 9
rs1367374 0.790 0.080 2 153074663 intergenic variant G/C snv 0.19 9
rs140355816 0.790 0.080 8 116562277 intergenic variant C/G snv 9.8E-03 9
rs1407508 0.790 0.080 9 98882256 regulatory region variant T/C snv 4.1E-02 9
rs1445011 0.790 0.080 5 40280100 intergenic variant T/C;G snv 9
rs1453514 0.790 0.080 16 16899146 intergenic variant A/G snv 0.16 9
rs1476570 0.790 0.080 6 29842083 intergenic variant G/A;T snv 0.37 9
rs16941835 0.790 0.080 16 86662114 intron variant G/C snv 0.20 9
rs17035289 0.790 0.080 4 105127134 intergenic variant T/C snv 0.25 9
rs1810502 0.790 0.080 20 50440951 intergenic variant C/T snv 0.49 9
rs1871438 0.790 0.080 15 92316651 intron variant A/G snv 0.44 9
rs1886450 0.790 0.080 13 73412491 upstream gene variant A/G snv 0.65 9
rs2189261 0.790 0.080 8 90159507 intergenic variant G/A snv 0.64 9
rs2193352 0.790 0.080 10 99586852 intergenic variant A/G snv 0.15 9