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
rs12198173 0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 8
rs2516509 0.882 0.160 6 31482217 intron variant T/C snv 0.19 7
rs9368699 0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 7
rs1235162 0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs2284178 0.925 0.120 6 31464348 non coding transcript exon variant C/T snv 0.44 6