Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12952581 0.925 0.080 17 49370984 intron variant G/A snv 0.42 0.28 3
rs12722502 0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 4
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs11603634 1.000 0.080 11 1142570 intergenic variant A/G snv 0.38 2
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs11071559 0.925 0.080 15 60777789 intron variant C/T snv 0.23 4
rs10905284 0.882 0.200 10 8073399 intron variant C/A;T snv 4
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs1059513 0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs10455025 1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 3