Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs605066 6 139508529 intron variant C/T snv 0.53 4
rs998584 6 43790159 downstream gene variant C/A snv 0.41 4
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 3
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 3
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 3
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 3
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 3
rs10019888 4 26061368 regulatory region variant A/G snv 0.17 2
rs12061508 1.000 0.040 1 196615338 intergenic variant G/A snv 0.23 2
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 2
rs12714415 2 651430 intergenic variant T/C snv 0.19 2
rs1457489 1.000 0.080 18 60194728 upstream gene variant G/A snv 0.29 2
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 2
rs634869 6 139510620 intron variant T/A;C snv 2
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 2
rs1034207 6 127016554 intron variant C/A;G;T snv 0.94 1
rs11154370 6 126846446 intron variant A/G;T snv 1
rs1443512 12 53948900 downstream gene variant A/C;T snv 1
rs17568628 5 76751114 intergenic variant T/C;G snv 1
rs2119690 8 20002028 intergenic variant G/A;C snv 1
rs2145272 20 6645571 intergenic variant G/A;T snv 1
rs4580892 6 127088737 intron variant C/T snv 0.32 1
rs4846567 1 219577375 regulatory region variant G/T snv 0.23 1