Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10038095 5 75341886 intron variant A/T snv 0.38 3
rs10045497 5 75340659 intron variant C/A snv 0.35 1
rs1006725 10 112970444 intron variant A/G snv 4.2E-03 2
rs10087178 8 10111284 intron variant T/C snv 6.6E-02 2
rs10102164
RP1
8 54509054 upstream gene variant G/A snv 0.19 3
rs10107815 8 10156645 intron variant G/C snv 5.1E-02 4
rs10128711 11 18611437 intron variant T/C snv 0.64 0.55 1
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 4
rs1016988 5 132408882 upstream gene variant T/C snv 0.20 3
rs10199768 2 21021128 intron variant G/T snv 0.35 5
rs10212320 3 30632373 non coding transcript exon variant C/T snv 7.2E-03 2
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs10260606 7 44544952 upstream gene variant G/A;C snv 2
rs10271556 7 106258428 intron variant C/T snv 5.6E-02 4
rs10306121 9 122372369 intron variant A/T snv 6.5E-02 2
rs10306137 9 122376185 intron variant C/T snv 1.8E-02 3
rs1038026 1.000 0.080 19 44901805 3 prime UTR variant A/G;T snv 1
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 6
rs10402729 19 19244291 intron variant T/C snv 3.3E-02 4
rs10415849 19 19394278 intron variant C/T snv 0.12 4
rs1041968 2 21009932 synonymous variant G/A snv 0.39 0.38 4
rs1042031 0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 3
rs1042034 0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 7
rs10433493 3 190647811 intron variant G/C snv 1.8E-02 2