Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3846662 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 12
rs12916 0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 12
rs12654264 0.925 0.120 5 75352778 intron variant A/T snv 0.38 7
rs3846663 0.882 0.120 5 75359901 intron variant C/T snv 0.35 7
rs17238484 1.000 0.080 5 75352671 intron variant G/T snv 0.22 4
rs3761740 0.882 0.160 5 75336308 intron variant C/A snv 8.2E-02 4
rs10038095 5 75341886 intron variant A/T snv 0.38 3
rs10474434 5 75348856 intron variant G/T snv 0.20 3
rs3761739 5 75335676 intron variant C/T snv 0.15 3
rs6453131 5 75348881 intron variant T/G snv 0.39 3
rs4629571 0.925 0.160 5 75362479 intron variant A/G snv 8.7E-02 2
rs10045497 5 75340659 intron variant C/A snv 0.35 2
rs3843482 5 75343434 intron variant T/G snv 0.35 2
rs17238540 1.000 0.040 5 75359673 non coding transcript exon variant T/G snv 4.0E-02 2
rs3846661 5 75343353 intron variant A/G snv 0.56 1