Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10182181 1.000 0.080 2 24927427 intergenic variant A/G snv 0.57 1
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 1
rs11041816 11 8222251 downstream gene variant A/G snv 0.36 1
rs11127485 1.000 0.080 2 632028 intergenic variant C/T snv 0.85 1
rs12198798 6 12509895 upstream gene variant T/C snv 0.17 1
rs12422552 0.925 0.080 12 14260997 regulatory region variant G/C snv 0.30 1
rs12955983 1.000 0.080 18 60205756 intergenic variant A/G snv 0.20 1
rs1564981 16 50952397 intergenic variant G/A snv 0.60 1
rs1582931 5 123321505 intergenic variant G/A;T snv 1
rs17150703 1.000 0.080 8 9888288 intergenic variant G/A snv 8.5E-02 1
rs2145270 20 6641038 regulatory region variant C/T snv 0.61 1
rs2145272 20 6645571 intergenic variant G/A;T snv 1
rs2207139 1.000 0.080 6 50877777 intergenic variant A/G snv 0.16 1
rs2351774 2 203234499 upstream gene variant A/G snv 0.46 1
rs2546057 1.000 0.040 19 33829949 intergenic variant A/C snv 0.41 1
rs2968864 7 150925074 intergenic variant T/C snv 0.16 1
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 1
rs4735692 1.000 0.080 8 75703428 intergenic variant A/G snv 0.48 1
rs518785 1 110817180 regulatory region variant G/A snv 0.82 1
rs645040 3 136207780 upstream gene variant G/T snv 0.77 1
rs6711012 1.000 0.080 2 624034 intergenic variant G/A;C;T snv 1
rs6752378 1.000 0.080 2 24927247 intergenic variant C/A snv 0.57 1
rs7374732 1.000 0.080 3 23161963 regulatory region variant C/T snv 0.73 1
rs7534091 1 118321993 intergenic variant A/G snv 0.23 1
rs9568867 1.000 0.080 13 53533217 intron variant G/A snv 0.13 1