Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17277546 7 99891948 3 prime UTR variant G/A snv 3.1E-02 4
rs4481233 0.925 0.120 4 9954455 intron variant C/T snv 0.16 5
rs1447352 11 92989595 downstream gene variant G/A snv 0.55 2
rs4905014 0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs11185790 10 89612776 intron variant G/A snv 0.15 3
rs494562 6 85407411 intergenic variant A/G snv 0.16 2
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs211718 1 75640990 downstream gene variant T/C snv 0.75 3
rs5744680 0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs4704221 0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs13391552 2 73591809 intron variant G/A;C snv 2
rs2074755 0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs7190256 0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs6499165 16 68292297 non coding transcript exon variant A/C snv 0.80 2
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 3
rs4329
ACE
17 63486097 intron variant A/C;G snv 2
rs2652822 15 63130573 3 prime UTR variant T/C snv 0.41 2
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs7094971 0.925 0.120 10 59689806 intron variant A/G snv 0.13 4
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20