Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2997119 0.882 0.040 13 55819766 intergenic variant A/G snv 0.52 3
rs4380187 0.925 0.040 2 184947213 intergenic variant A/C snv 0.34 3
rs4949526 1.000 0.040 1 29959372 intergenic variant T/C snv 0.54 3
rs506597 0.882 0.040 7 100715797 upstream gene variant A/G snv 0.90 3
rs55771711 1.000 0.040 10 131989233 intergenic variant G/C snv 0.24 3
rs55834529 0.882 0.120 6 27104763 intergenic variant A/G snv 4.9E-02 3
rs56196471 0.882 0.040 4 178642661 intergenic variant G/A snv 2.9E-02 3
rs59721556 1.000 0.040 14 77646050 TF binding site variant G/A snv 0.19 3
rs62482377 0.882 0.040 7 156250946 intergenic variant G/C snv 0.10 3
rs6940116 1.000 0.040 6 27740953 upstream gene variant A/G snv 0.18 3
rs7405404 0.925 0.040 16 13656002 intergenic variant T/A;C snv 3
rs7766730 0.882 0.040 6 65987110 intergenic variant C/A;T snv 3
rs77867520 0.882 0.040 4 11186225 intergenic variant C/T snv 7.2E-02 3
rs911186 0.925 0.040 6 27182820 intergenic variant A/G snv 0.25 3
rs9354352 0.882 0.040 6 65986379 intergenic variant T/C snv 0.42 3
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 3
rs1008078 1.000 0.040 1 90724174 non coding transcript exon variant C/T snv 0.33 2
rs10757417 1.000 0.040 9 23347855 intron variant G/A;T snv 2
rs1076884 1.000 0.040 16 13653946 intergenic variant C/G;T snv 2
rs10791106 1.000 0.040 11 130976537 intergenic variant A/G snv 0.45 2
rs10791111 1.000 0.040 11 130986204 intergenic variant T/G snv 0.45 2
rs1080500 1.000 0.040 3 53141001 intergenic variant G/A snv 0.27 2
rs10994707 1.000 0.040 10 61291201 intergenic variant T/A snv 0.10 2
rs10995426 1.000 0.040 10 63080258 intergenic variant T/C snv 0.41 2
rs11223651 1.000 0.040 11 133971139 intergenic variant C/T snv 0.16 2