Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs3130380 0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs9261290 0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs185819 0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 8
rs2269426 0.807 0.280 6 32108722 intron variant G/A snv 0.35 8
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 7
rs6457374 0.851 0.200 6 31304484 intron variant C/T snv 0.81 7
rs2523554 0.925 0.080 6 31364052 upstream gene variant C/T snv 0.70 5