Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10054063 5 173965395 downstream gene variant A/T snv 0.26 4
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 4
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 4
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 4
rs12272004 1.000 0.040 11 116733008 TF binding site variant C/A snv 9.8E-02 4
rs13392272 2 20994618 downstream gene variant C/T snv 0.37 4
rs1495743 8 18415790 intergenic variant G/A;C snv 4
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 4
rs176813 4 68733813 regulatory region variant T/C snv 0.38 4
rs2207132 20 40513876 intergenic variant G/A snv 2.7E-02 4
rs2954022 8 125470379 intron variant C/A;T snv 4
rs2980875 8 125469505 intron variant A/C;G;T snv 4
rs4564803 2 20982630 intergenic variant G/T snv 0.25 4
rs4850047 2 3587163 regulatory region variant T/C snv 0.84 4
rs4870941 8 125486586 intron variant G/C snv 0.20 4
rs5014650 6 160678471 upstream gene variant G/A snv 0.16 4
rs509728 11 116662450 downstream gene variant G/C snv 2.7E-02 4
rs56156922 16 56953457 intergenic variant T/C snv 0.26 4
rs5942937 X 110473179 intron variant T/G snv 0.47 4
rs5985471 X 110460733 downstream gene variant C/T snv 0.43 4
rs668948 1.000 0.040 2 21068657 regulatory region variant G/A snv 0.71 4
rs6855363 4 156749385 intergenic variant T/A;C snv 4
rs71559014 6 27154665 regulatory region variant A/G snv 4.2E-02 4
rs1030431 8 58399138 intergenic variant A/G;T snv 3
rs10761716 10 63122540 downstream gene variant C/G snv 0.40 3