Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 4
rs12696304 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 4
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 4
rs4968782 1.000 0.080 17 63471115 upstream gene variant G/A;T snv 4
rs1483121 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 3
rs157595 1.000 0.080 19 44922203 upstream gene variant A/G;T snv 3
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 3
rs75627662 1.000 0.080 19 44910319 non coding transcript exon variant C/T snv 0.17 3
rs759819 1.000 0.080 19 54304302 intron variant C/G;T snv 3
rs10222981 0.925 0.080 4 6759326 upstream gene variant G/T snv 0.14 2
rs10792832 1.000 0.080 11 86156833 downstream gene variant A/G snv 0.70 2
rs117905930 1.000 0.080 9 88973603 intron variant C/A;T snv 2
rs12805422 1.000 0.080 11 45818338 intron variant G/A snv 0.42 2
rs141622900 1.000 0.080 19 44923535 upstream gene variant G/A snv 5.9E-02 2
rs147906088 1.000 0.080 7 54496119 intergenic variant C/A;T snv 2
rs17090219 0.925 0.080 18 56523802 intergenic variant T/C snv 7.4E-02 2
rs2525776 0.925 0.080 7 81272303 intergenic variant C/T snv 0.19 2
rs28868104 1.000 0.080 3 104241993 intergenic variant C/T snv 0.17 2
rs365521 0.925 0.080 17 62944934 intron variant A/G snv 0.62 2
rs4576506 0.925 0.120 9 31546474 intergenic variant A/G snv 0.91 2
rs58826447 1.000 0.080 19 44825122 downstream gene variant T/A;G snv 2
rs61835453 0.925 0.080 10 2717604 intergenic variant T/C snv 5.8E-02 2
rs62117160 0.925 0.120 19 44728895 upstream gene variant G/A;T snv 2
rs6931277 0.925 0.200 6 32615580 regulatory region variant A/T snv 0.15 2
rs7113976 1.000 0.080 11 86158695 regulatory region variant C/T snv 0.44 2