Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35062987 6 32622958 TF binding site variant C/T snv 0.22 1
rs3800406 6 35165297 regulatory region variant A/G snv 7.7E-02 1
rs4938303 11 116714271 intergenic variant C/A;T snv 0.62 1
rs4942859 13 49624022 upstream gene variant G/A snv 0.49 1
rs558971 1 234717659 intron variant A/G snv 0.65 1
rs55935382 7 50250073 intron variant C/A snv 0.27 1
rs57594838 10 112265424 intergenic variant T/G snv 0.24 1
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 1
rs626913 8 60635935 non coding transcript exon variant A/C;T snv 1
rs6448771 4 31395996 intergenic variant G/A;C snv 1
rs6579245 20 35537447 upstream gene variant C/T snv 0.16 1
rs6656611 1 16189310 regulatory region variant T/C snv 0.51 1
rs672889 2 21096144 intron variant T/G snv 0.80 1
rs6944635 7 46132286 regulatory region variant A/G snv 0.28 1
rs6982636 8 125467073 intron variant G/A snv 0.43 1
rs6987702 8 125492484 intron variant T/C snv 0.43 1
rs71435601 2 21205417 intergenic variant A/G snv 0.10 1
rs7214248 17 30247159 intron variant G/A snv 0.31 1
rs73015024 19 11086922 upstream gene variant G/T snv 0.12 1
rs7396835 11 116813312 non coding transcript exon variant T/A;C;G snv 1
rs75542613 11 116808439 downstream gene variant G/A snv 5.6E-02 1
rs7575840 1.000 0.040 2 21050618 intergenic variant G/T snv 0.26 1
rs7641325 3 12227104 intergenic variant G/A snv 0.47 1
rs7927208 11 122636262 intergenic variant T/A;C snv 1
rs8106503 19 11086210 upstream gene variant T/C snv 0.16 1