Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11753207 1.000 0.040 6 32584671 intron variant A/C snv 0.12 2
rs142790902 1.000 0.040 6 32582137 intron variant T/C snv 6.0E-02 2
rs144660248 1.000 0.040 6 32583926 intron variant G/T snv 2
rs2760981 1.000 0.040 6 32597688 intergenic variant G/A;C;T snv 2
rs28724212 1.000 0.040 6 32588824 intron variant A/G snv 2
rs41293179 1.000 0.040 6 32582101 intron variant C/G;T snv 2
rs9270074 1.000 0.040 6 32586352 intron variant T/C snv 2