Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
rs1953126 1.000 0.120 9 120878222 intron variant T/C snv 0.68 2
rs13031237
REL
1.000 0.120 2 60908994 intron variant G/T snv 0.25 1
rs17066096 1.000 0.080 6 137131771 intergenic variant A/G snv 0.20 1
rs2108225 1.000 0.040 7 107812658 downstream gene variant G/A;T snv 1
rs212402 1.000 0.080 6 159051263 intron variant G/A snv 0.66 1
rs2280141 1.000 0.040 10 122433665 3 prime UTR variant T/G snv 0.56 1
rs4648356 1.000 0.080 1 2792599 intron variant C/A snv 0.39 1
rs6726160 1.000 0.080 2 60937594 non coding transcript exon variant T/G snv 0.47 1
rs6848139 1.000 0.040 4 122473886 intergenic variant A/C;G snv 1
rs7523907 1.000 0.080 1 167458010 non coding transcript exon variant C/A;T snv 1
rs1131017 0.925 0.160 12 56042145 5 prime UTR variant C/A;G;T snv 8.0E-06; 8.0E-06; 0.62; 1.1E-04 3
rs6933404 0.925 0.280 6 137638098 intergenic variant T/C snv 0.16 3
rs864537 0.925 0.200 1 167442147 intron variant A/G snv 0.29 3
rs2281808 0.925 0.160 20 1629905 intron variant T/A;C snv 2
rs2456973 0.925 0.040 12 56023144 intron variant A/C;G snv 2
rs3890745 0.925 0.200 1 2622185 intron variant T/C snv 0.40 2
rs6859219 0.925 0.160 5 56142753 intron variant C/A snv 0.20 2
rs10892258 0.925 0.120 11 118709156 intron variant G/A snv 0.19 1
rs11676922 0.925 0.160 2 100190478 intron variant T/A snv 0.51 1
rs13315591 0.925 0.160 3 58571114 intron variant T/C snv 0.15 1
rs13390936 0.925 0.080 2 191090090 intron variant A/T snv 8.4E-02 1
rs1800907 0.925 0.120 7 142800425 upstream gene variant T/C snv 0.56 1
rs212389 0.925 0.160 6 159068759 non coding transcript exon variant G/A snv 0.60 1
rs231804 0.925 0.200 2 203843923 intergenic variant C/T snv 0.60 1