Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80333777 1.000 0.080 5 15524361 intron variant G/A;C;T snv 2
rs112284299 1.000 0.080 3 179850308 intron variant G/C snv 1.6E-02 2
rs6847878 1.000 0.080 4 81419698 intergenic variant G/T snv 9.1E-03 2
rs113816795 1.000 0.080 5 99159794 intergenic variant T/C snv 8.1E-03 2
rs116616455 1.000 0.080 12 58041829 intergenic variant T/C snv 1.4E-02 2
rs58847779 1.000 0.080 22 37736644 intron variant T/C snv 4.4E-02 2
rs6693796 1.000 0.080 1 170674137 intron variant T/C snv 7.7E-02 2
rs4988198 1.000 0.080 2 135861240 intron variant T/C;G snv 2
rs7810240 1.000 0.080 7 150387372 intron variant T/C;G snv 2
rs138270994 1.000 0.080 13 22791997 intergenic variant TCTTTG/- delins 2.3E-02 2