Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 10
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 8
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 6
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs3130350 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 5
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 5
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 5
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 5
rs10484399 0.851 0.240 6 27566749 intergenic variant A/G snv 5.4E-02 4
rs1394371 0.925 0.080 15 78432127 intergenic variant C/T snv 0.22 4
rs2746150 0.851 0.240 6 29474924 downstream gene variant C/T snv 5.3E-02 4
rs2844659 0.851 0.280 6 30856755 intergenic variant C/G;T snv 4
rs4887053 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 4
rs1233579 0.925 0.160 6 28744886 intergenic variant A/G snv 7.2E-02 3
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 3
rs3130893 0.882 0.160 6 29012930 intergenic variant A/G snv 5.3E-02 3
rs3131093 0.925 0.160 6 28869660 intergenic variant C/T snv 7.1E-02 3
rs1846594 0.925 0.120 3 113197356 intergenic variant G/A;T snv 2
rs2596571 0.925 0.160 6 31380245 upstream gene variant G/C snv 0.74 2
rs3094694 0.925 0.200 6 30484127 upstream gene variant T/C snv 0.16 2
rs35755165 0.882 0.080 19 40840084 intron variant A/C;G snv 2
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 2
rs9295740 0.827 0.120 6 27721723 intergenic variant G/A snv 0.27 2