Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10277986 1.000 0.120 7 50961290 intron variant T/A;C snv 1
rs11170445 1.000 0.120 12 53151908 upstream gene variant C/T snv 0.33 1
rs11954020 1.000 0.120 5 35883149 downstream gene variant C/G;T snv 1
rs12251307 1.000 0.120 10 6081532 intergenic variant C/T snv 0.18 1
rs12444268 1.000 0.120 16 20331250 upstream gene variant T/A snv 0.22 1
rs12453507 0.925 0.200 17 39896954 intergenic variant C/G;T snv 1
rs2085277 1.000 0.120 13 31593580 intergenic variant A/T snv 2.2E-02 1
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 1
rs2517532 0.925 0.120 6 31050630 upstream gene variant A/G snv 0.60 1
rs2611215 1.000 0.120 4 165653115 intron variant A/G snv 0.83 1
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 1
rs3095340 1.000 0.120 6 30759162 intron variant A/C snv 0.16 1
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 1
rs3135338 0.882 0.240 6 32433440 regulatory region variant C/T snv 0.62 1
rs3957146 0.882 0.200 6 32713753 upstream gene variant T/C snv 9.1E-02 1
rs4459609 0.925 0.120 17 63471587 upstream gene variant C/A snv 0.63 1
rs4622308 0.925 0.160 12 56075401 upstream gene variant C/T snv 1
rs4900384 0.882 0.160 14 98032614 intergenic variant A/G snv 0.40 1
rs4948088 0.925 0.160 7 50959497 intron variant A/C snv 0.96 1
rs507778 0.925 0.200 6 32242084 intergenic variant C/T snv 0.38 1
rs549182 0.925 0.160 6 32237268 intergenic variant G/A snv 4.5E-02 1
rs5790666 1.000 0.120 11 27778324 intron variant G/- delins 0.14 1
rs5979785 0.925 0.160 X 12953405 intergenic variant C/T snv 1
rs6547853 1.000 0.120 2 28423934 upstream gene variant G/A snv 0.35 1
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 1