Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 10
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 6
rs6932542 0.827 0.200 6 32412485 downstream gene variant A/G snv 0.55 5
rs9880772 0.827 0.240 3 27736288 intergenic variant G/A snv 0.59 5
rs4240807 0.851 0.160 16 85951755 downstream gene variant A/C snv 0.76 4
rs9296015 0.851 0.280 6 32251212 upstream gene variant G/A snv 0.22 4
rs9392017 0.851 0.160 6 442357 intergenic variant G/A;C snv 4
rs649775 0.882 0.120 6 33716536 upstream gene variant A/G;T snv 3
rs13195441 0.925 0.200 6 32775521 intergenic variant G/A snv 0.30 2
rs181997 0.925 0.160 6 32932941 downstream gene variant G/A;C snv 2
rs3129214 0.925 0.160 6 33149481 downstream gene variant C/T snv 0.24 2
rs4959089 0.925 0.200 6 32251948 upstream gene variant A/G snv 0.22 2
rs6901221 0.925 0.160 6 33130499 downstream gene variant A/C snv 0.13 2
rs756440 0.925 0.160 6 33154554 intergenic variant A/G snv 0.24 2
rs1002658 1.000 0.120 6 137660447 intron variant C/T snv 0.15 1
rs3093998 1.000 0.120 6 31517397 downstream gene variant C/A snv 0.70 1
rs3130237 1.000 0.120 6 33129784 downstream gene variant T/C snv 0.13 1
rs6565176 1.000 0.120 16 30163605 intergenic variant T/A;C snv 1
rs9267947 1.000 0.120 6 32243441 intergenic variant A/G;T snv 1