Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs1893592 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs5743618 0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 6
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 5
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs61816761 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 5
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs7512552 1.000 0.120 1 150293284 upstream gene variant T/C snv 0.63 4
rs9368699 0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 4
rs1295685 0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 4
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 3
rs10791824 0.882 0.160 11 65791795 intron variant A/G;T snv 3
rs6010620 0.701 0.360 20 63678486 intron variant A/C;G snv 3
rs1295686 0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 3
rs12081541 0.925 0.160 1 152468890 intergenic variant T/C snv 8.9E-02 2
rs1384974 0.925 0.120 3 177009491 downstream gene variant T/C snv 9.6E-02 2
rs1528473 0.925 0.120 15 55094545 downstream gene variant A/G snv 7.6E-02 2
rs17728338 0.851 0.160 5 151098757 downstream gene variant G/A snv 7.1E-02 2
rs67766926 0.925 0.120 2 60936446 downstream gene variant C/G snv 0.17 2
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 2
rs9302874 0.925 0.120 17 78284479 intergenic variant C/T snv 0.24 2