Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 8
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 8
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 7
rs7681423 4 154621096 intergenic variant C/T snv 0.26 5
rs12061601 1.000 0.040 1 169101212 intron variant T/C snv 0.16 3
rs502361 9 133280016 upstream gene variant G/C snv 0.26 3
rs633862 0.925 0.120 9 133279871 upstream gene variant T/C snv 0.49 3
rs10737547 1 169506814 intergenic variant A/G snv 0.93 2
rs12644950 4 154616169 upstream gene variant G/A snv 0.25 2
rs13109457 4 154593727 upstream gene variant G/A snv 0.25 2
rs13130318 4 154617318 upstream gene variant T/G snv 0.23 2
rs1894692 1 169498416 non coding transcript exon variant G/A snv 0.98 2
rs500428 9 133279770 upstream gene variant G/A snv 0.26 2
rs552148 9 133278037 upstream gene variant C/T snv 0.25 2
rs558240 9 133281560 intergenic variant G/A snv 0.33 2
rs6687813 1 169508336 downstream gene variant A/C snv 0.93 2
rs6696217 1 169491488 non coding transcript exon variant A/G snv 0.92 2
rs7654093 0.882 0.120 4 154623920 upstream gene variant A/T snv 0.27 2
rs7659024 4 154599778 downstream gene variant G/A snv 0.26 2
rs819131 20 34320043 intergenic variant G/A snv 0.87 2
rs970740 1 169510736 downstream gene variant C/T snv 0.95 2
rs10476160 5 175547573 regulatory region variant A/G;T snv 1
rs141237278 11 47899441 regulatory region variant G/T snv 1.2E-02 1