Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11961710 1.000 0.080 6 113399037 intergenic variant G/A snv 3.2E-02 1
rs11967676 1.000 0.080 6 48747159 regulatory region variant A/G snv 0.12 1
rs12041233 1.000 0.080 1 37287106 intron variant G/A snv 6.6E-02 1
rs123187 1.000 0.080 19 45327689 upstream gene variant G/A snv 0.51 1
rs12334143 1.000 0.080 7 85553700 regulatory region variant T/C snv 0.33 1
rs12374991 1.000 0.080 7 11188315 intron variant G/T snv 6.3E-02 1
rs12378800 1.000 0.080 9 97869538 regulatory region variant G/A;T snv 1
rs12798898 1.000 0.080 11 85948537 intergenic variant A/G snv 1.0E-01 1
rs13133687 1.000 0.080 4 168062923 intron variant G/A snv 2.9E-02 1
rs13178362 1.000 0.080 5 30178906 intergenic variant T/C snv 0.17 1
rs13241213 1.000 0.080 7 50255260 intron variant C/G;T snv 1
rs138090874 1.000 0.080 7 31262777 intergenic variant G/A snv 9.8E-03 1
rs138098194 1.000 0.080 18 66840171 intergenic variant G/A snv 6.4E-03 1
rs138235833 1.000 0.080 19 44912028 non coding transcript exon variant T/G snv 3.0E-02 1
rs140009341 1.000 0.080 2 136433314 intergenic variant G/A;C snv 1
rs140233081 1.000 0.080 7 541098 intergenic variant C/A;T snv 7.7E-02 1
rs140633572 1.000 0.080 6 106832060 intergenic variant A/G snv 5.3E-02 1
rs141503849 1.000 0.080 22 19704370 regulatory region variant C/T snv 6.3E-03 1
rs142176337 1.000 0.080 18 59914255 intergenic variant T/C snv 4.0E-03 1
rs1422438 1.000 0.080 5 107775475 intergenic variant G/C;T snv 1
rs143083071 1.000 0.080 1 99242198 intron variant G/A snv 3.1E-03 1
rs143638193 1.000 0.080 4 140579551 non coding transcript exon variant C/G;T snv 1
rs143766413 1.000 0.080 5 154557919 downstream gene variant G/C snv 1.4E-05 1
rs1443024 1.000 0.080 2 184511570 intergenic variant T/A snv 0.29 1
rs144311893 1.000 0.080 19 44920687 downstream gene variant C/T snv 1.3E-02 1