Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs11465804 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs7517847 0.689 0.600 1 67215986 intron variant T/G snv 0.37 2
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 2
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs2516049 0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs2247056 0.882 0.160 6 31297713 intron variant T/C snv 0.80 8
rs389884 0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 7
rs477515 0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 7
rs3117582 0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 6
rs2076530 0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 5
rs2239804 0.851 0.240 6 32443746 intron variant T/A;C snv 0.51 5
rs2395157 0.827 0.240 6 32380368 intron variant A/G snv 0.24 5
rs2395182 0.851 0.280 6 32445540 downstream gene variant G/T snv 0.76 5
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs3177928 0.882 0.120 6 32444658 3 prime UTR variant G/A snv 0.13 5
rs3817963 0.776 0.360 6 32400310 intron variant T/C snv 0.25 5
rs615672 0.851 0.240 6 32606394 intergenic variant G/A;C snv 5
rs6932542 0.827 0.200 6 32412485 downstream gene variant A/G snv 0.55 5
rs7194 0.827 0.280 6 32444703 3 prime UTR variant G/A snv 0.61 5
rs1480380 0.763 0.360 6 32945469 intron variant C/T snv 0.11 4
rs2227139 0.925 0.160 6 32445682 downstream gene variant G/A snv 0.61 4
rs3129768 0.851 0.240 6 32627306 upstream gene variant G/T snv 0.76 4