Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1008953 1.000 0.040 20 45352086 upstream gene variant T/C snv 0.79 1
rs10794648 1.000 0.040 1 24191716 upstream gene variant T/C snv 0.68 1
rs10960680 1.000 0.040 9 12483941 intergenic variant A/C snv 9.4E-02 1
rs11135056 1.000 0.040 5 159260273 upstream gene variant C/T snv 0.27 1
rs114934997 1.000 0.040 5 40370622 intergenic variant C/A;T snv 1
rs12118303 1.000 0.040 1 172705957 intergenic variant T/C snv 0.14 1
rs12119179 0.925 0.200 1 67281732 downstream gene variant A/C snv 0.30 1
rs12458130 1.000 0.040 18 8667063 intergenic variant G/A snv 8.9E-02 1
rs12580100 1.000 0.040 12 56045425 upstream gene variant A/G snv 0.14 1
rs12650590 1.000 0.040 4 155618869 intergenic variant G/T snv 0.14 1
rs13437088 0.925 0.040 6 31387342 intergenic variant C/T snv 0.32 1
rs1581803 1.000 0.040 1 152619805 downstream gene variant G/T snv 0.58 1
rs2082412 0.925 0.120 5 159290781 downstream gene variant G/A snv 0.27 1
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 1
rs4085613 0.827 0.160 1 152577542 downstream gene variant T/G snv 0.59 1
rs4112788 0.851 0.120 1 152578800 downstream gene variant A/G;T snv 1
rs4319543 1.000 0.040 12 122160501 intergenic variant A/C snv 0.35 1
rs4379175 1.000 0.040 5 159377920 intron variant G/T snv 0.36 1
rs4649203 0.851 0.160 1 24193430 intergenic variant G/A snv 0.61 1
rs4722404 0.851 0.120 7 3089155 intron variant T/C snv 0.40 1
rs4845454 0.925 0.040 1 152619708 downstream gene variant C/A;T snv 1
rs4845459 1.000 0.040 1 152631366 intergenic variant C/A;G snv 1
rs4921493 0.925 0.080 5 159409099 intron variant T/A;C snv 1
rs514475 1.000 0.040 6 137717768 intron variant A/C snv 0.90 1
rs6020157 1.000 0.040 20 49975221 downstream gene variant G/A snv 0.29 1