Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12914385 0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs2869967 0.827 0.120 4 88948181 intron variant T/C snv 0.49 5
rs4416442 0.925 0.080 4 88945562 intron variant T/C snv 0.45 4
rs114931935 0.925 0.080 1 161690011 upstream gene variant G/A snv 3.0E-02 2
rs12692398 0.925 0.080 2 10060189 intron variant G/A snv 0.17 2
rs12910412 0.925 0.080 15 94163844 upstream gene variant T/G snv 0.37 2
rs139257032 0.925 0.080 2 119571288 intron variant C/T snv 1.6E-02 2
rs142700918 0.925 0.080 8 3448320 intron variant G/A snv 5.8E-03 2
rs34391416 0.925 0.080 11 831818 3 prime UTR variant G/A snv 2.7E-02 2