Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11236213 11 74683324 upstream gene variant G/A snv 0.26 1
rs11263432 11 69432586 downstream gene variant T/C snv 0.50 1
rs112938313 6 84999770 intergenic variant A/G snv 6.8E-02 1
rs114760566 6 34224259 downstream gene variant C/A snv 2.5E-02 1
rs1152008 3 12446113 intergenic variant T/G snv 0.45 1
rs11534749 12 26312579 intron variant T/A;G snv 1
rs115381724 3 12274264 intergenic variant A/G snv 1.4E-02 1
rs1156979 3 89081667 intergenic variant A/T snv 0.49 1
rs1158805 18 43156625 intergenic variant C/A snv 0.45 1
rs1163627 13 111573354 regulatory region variant C/A snv 0.58 1
rs11654387 17 70450720 intergenic variant C/G;T snv 1
rs117595678 9 124829194 intergenic variant C/T snv 9.1E-02 1
rs1182864 6 39262531 intergenic variant G/A snv 0.28 1
rs11881865 19 12988179 regulatory region variant G/C snv 0.13 1
rs11992444 8 25607174 intron variant G/T snv 0.49 1
rs12061508 1.000 0.040 1 196615338 intergenic variant G/A snv 0.23 1
rs12112380 7 30896285 intron variant T/C snv 0.12 1
rs12162221 19 18524579 upstream gene variant G/A;C snv 1
rs12361415 11 47452594 upstream gene variant T/G snv 0.20 1
rs12419064 11 10299061 upstream gene variant A/G snv 0.44 1
rs12435790 14 34685175 regulatory region variant A/G snv 6.4E-02 1
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 1
rs12450700 17 67372783 upstream gene variant T/G snv 0.27 1
rs12593088 15 80766299 downstream gene variant G/A snv 0.22 1
rs12629247 3 187914796 intergenic variant G/C snv 3.1E-02 1