Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10024899 4 121705035 intergenic variant T/C snv 0.35 1
rs10070064 5 173854774 intergenic variant C/T snv 0.26 1
rs10458575 1 65104082 regulatory region variant T/C snv 0.45 1
rs10464079 5 179098778 intergenic variant G/A snv 0.71 1
rs10475249 5 4010021 downstream gene variant C/G snv 0.45 1
rs10490869 3 35593653 intergenic variant A/T snv 0.15 1
rs10501039 11 26152856 intergenic variant T/C snv 4.5E-02 1
rs10507223 12 108062051 intergenic variant C/G snv 0.17 1
rs10763957 10 33877770 regulatory region variant C/T snv 0.35 1
rs10827252 10 33383956 upstream gene variant A/G snv 0.51 1
rs10844642 12 33577433 downstream gene variant A/C snv 0.27 1
rs10851523 15 52751805 downstream gene variant G/A;C snv 1
rs10880321 12 37976308 intergenic variant C/A;G snv 1
rs10991433 9 104964637 intergenic variant T/C snv 8.2E-02 1
rs10992408 9 92682518 intergenic variant A/G snv 0.20 1
rs10993017 9 93998102 intergenic variant T/A;C snv 0.31 1
rs11055887 12 14264245 intergenic variant G/A snv 0.14 1
rs11059476 12 122708052 intron variant C/T snv 3.9E-02 1
rs11176015 12 66047904 intergenic variant C/T snv 0.32 1
rs11187140 10 92707153 downstream gene variant G/A snv 0.29 1
rs11187742 10 93966124 upstream gene variant A/G;T snv 1
rs11202585 10 87849022 downstream gene variant G/C snv 0.18 1
rs1122080 5 158588895 downstream gene variant G/A snv 0.21 1
rs1122157 10 62101841 downstream gene variant C/A;T snv 1
rs112266013 6 15230512 intergenic variant G/A snv 0.12 1