Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 5
rs2927438 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 5
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 5
rs675504 11 102959002 upstream gene variant A/G snv 0.98 5
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 4
rs16860926 3 186609982 intron variant T/C snv 2.6E-02 4
rs2523575 6 31361049 upstream gene variant C/G snv 0.20 4
rs585362 1 109247173 upstream gene variant C/G;T snv 4
rs754523 2 21088819 intergenic variant A/G snv 0.28 4
rs754524 2 21088669 intergenic variant T/G snv 0.19 4
rs10788994 1 55035303 upstream gene variant C/T snv 0.20 3
rs11577931 1 109278262 downstream gene variant A/G snv 5.5E-02 3
rs11925396 3 194391622 downstream gene variant A/G snv 1.9E-02 3
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 3
rs1713222 2 21048451 upstream gene variant A/G snv 0.82 3
rs17398765 2 21047879 upstream gene variant A/G snv 4.8E-02 3
rs2081687 0.882 0.240 8 58476006 intergenic variant T/C snv 0.70 3
rs2149041 1 55036464 upstream gene variant C/G snv 0.17 3
rs2182833 1 55034756 upstream gene variant A/G snv 0.23 3
rs4591370 2 21160870 intergenic variant A/G snv 0.75 3
rs4605275 1.000 0.080 19 44835236 intergenic variant T/C snv 0.69 3
rs506585 2 21174310 intergenic variant G/A;C;T snv 3
rs55882046 1 109277359 downstream gene variant C/T snv 6.7E-02 3
rs563290 2 21065354 intergenic variant G/A snv 0.69 3
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 3