Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 13
rs58658771 0.776 0.080 15 32709533 intergenic variant T/A snv 0.20 13
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 7
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs6475611 9 22151140 intergenic variant G/A snv 0.21 6
rs737092 20 57415349 regulatory region variant T/C snv 0.58 6
rs142550358 9 88777772 intron variant CT/- delins 3.9E-02 5
rs4672497 2 62296430 TF binding site variant C/G;T snv 5
rs6014993 20 57416581 regulatory region variant A/G snv 0.58 5
rs11021221 11 95575690 intron variant T/A;G snv 4
rs11756659 6 25933704 upstream gene variant A/G;T snv 4
rs12134279 0.925 0.080 1 197812068 regulatory region variant C/T snv 0.17 4
rs532591337 19 12459271 intron variant G/A snv 4.9E-05 4
rs62322662 0.925 0.080 4 122438414 intergenic variant A/G snv 5.1E-02 4
rs6684375 1 22379941 regulatory region variant C/T snv 0.20 4
rs739385 7 93053295 regulatory region variant G/A;C snv 4
rs74612091 9 133001891 intergenic variant T/A snv 7.7E-02 4
rs10011838 1.000 0.080 4 152599127 intergenic variant G/A snv 0.42 3
rs10099100 8 10719265 downstream gene variant G/C snv 0.32 3
rs11082513 18 46167187 intergenic variant C/T snv 0.42 3