Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5574 0.882 0.200 7 24289514 synonymous variant C/T snv 0.43 0.43 5
rs11178997 0.827 0.040 12 71938373 upstream gene variant T/A snv 0.12 5
rs9315202 0.925 0.080 13 33067879 downstream gene variant C/T snv 0.24 4
rs1876831 0.925 0.040 17 45830379 non coding transcript exon variant C/G;T snv 4.4E-06; 0.14 4
rs495225 0.882 0.040 3 172448243 synonymous variant G/A;C;T snv 0.66 4
rs9563121
KL
0.925 0.080 13 33050369 intron variant C/T snv 0.26 4
rs4792887 0.882 0.080 17 45799654 non coding transcript exon variant C/T snv 0.16 4
rs386231 0.882 0.080 1 162356033 intron variant C/T snv 0.68 4
rs17759843 0.882 0.080 22 21920372 3 prime UTR variant G/A snv 6.7E-02 4
rs4311
ACE
0.882 0.200 17 63483402 intron variant T/C snv 0.60 3
rs2400707 1.000 0.040 5 148825489 5 prime UTR variant A/G;T snv 3
rs12944712 0.925 0.040 17 45793781 intron variant G/A snv 0.35 3
rs12364283 0.925 0.080 11 113476233 upstream gene variant A/G snv 5.8E-02 3
rs7552841 0.925 0.160 1 55053079 intron variant C/T snv 0.32 3
rs8042149 0.882 0.160 15 60832754 intron variant T/G snv 0.44 3
rs16965628 0.882 0.040 17 30228407 intron variant G/C snv 0.14 3
rs2267735 0.925 0.120 7 31095890 intron variant C/G snv 0.47 2
rs1042357 0.925 0.040 17 7001742 synonymous variant T/C;G snv 0.59 2
rs1799923
CCK
0.925 0.040 3 42264802 5 prime UTR variant A/G snv 0.82 2
rs10055255 1.000 0.040 5 76968168 intron variant A/T snv 0.50 2
rs562010289 0.925 0.120 1 183227583 missense variant G/A;C snv 1.7E-04 2
rs6470292 1.000 0.040 8 124855801 intron variant A/G snv 0.17 2
rs683250 1.000 0.040 11 83565125 intron variant A/G;T snv 2
rs4775301 0.925 0.040 15 60834660 intron variant T/C;G snv 2
rs8024133 0.925 0.040 15 60838440 intron variant C/T snv 0.42 2