Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12654264 0.878 0.107 5 75352778 intron variant A/T snp 0.39 7
rs3846662 0.821 0.250 5 75355259 non coding transcript exon variant A/G snp 0.50 0.58 7
rs12916 0.878 0.143 5 75360714 3 prime UTR variant T/C snp 0.38 5
rs17238484 1.000 0.071 5 75352671 intron variant G/T snp 0.23 3
rs10038095 5 75341886 intron variant A/T snp 0.39 2
rs10045497 5 75340659 intron variant C/A snp 0.36 2
rs10474434 5 75348856 intron variant G/T snp 0.20 2
rs17238540 1.000 0.036 5 75359673 non coding transcript exon variant T/G snp 3.7E-02 2
rs3761739 5 75335676 intron variant C/T snp 0.16 2
rs3761740 1.000 0.071 5 75336308 intron variant C/A snp 8.1E-02 2
rs3846663 1.000 0.036 5 75359901 intron variant C/T snp 0.37 2
rs4629571 0.923 0.143 5 75362479 intron variant A/G snp 8.7E-02 2
rs6453131 5 75348881 intron variant T/G snp 0.40 2
rs3843482 5 75343434 intron variant T/G snp 0.37 1