Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9287604 2 236867522 intergenic variant G/C snv 0.62 5
rs9804550 11 5164863 intergenic variant T/A;C snv 5
rs10206089 2 61476184 intron variant G/A snv 4
rs11359909 3 128603031 intergenic variant G/- delins 0.89 4
rs13138355 4 82624823 upstream gene variant C/A;T snv 4
rs143699489 3 141208279 intergenic variant A/G snv 0.22 4
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 4
rs34293785 1 65671509 intergenic variant T/C snv 4
rs413141 19 6675978 downstream gene variant A/G snv 0.84 4
rs56232812 1 27859995 intergenic variant A/C snv 0.11 4
rs74612091 9 133001891 intergenic variant T/A snv 7.7E-02 4
rs7537229 1 56440602 intron variant G/A snv 0.92 4
rs9880192 1.000 0.040 3 128578726 upstream gene variant G/A;C snv 0.31 4
rs10466905 12 6393666 upstream gene variant G/A snv 0.21 3
rs1157008 9 88920798 regulatory region variant T/C;G snv 3
rs11642657 16 85982722 intron variant C/A;T snv 3
rs11735662 4 144104973 intron variant C/T snv 2.1E-02 3
rs13187922 5 142083096 intergenic variant C/T snv 0.48 3
rs1449263 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 3
rs1456896 0.882 0.200 7 50264865 upstream gene variant C/T snv 0.67 3
rs17005891 4 82626709 downstream gene variant G/A snv 0.15 3
rs218264 4 54542708 intergenic variant A/G;T snv 3
rs2710804 7 36044919 intron variant T/C snv 0.29 3
rs34776209 7 23473474 upstream gene variant C/T snv 0.18 3
rs72801474 5 133108436 downstream gene variant G/A snv 5.2E-02 3