Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1194919682 0.925 0.040 2 136115158 missense variant A/G snv 2
rs761937143 1.000 0.040 18 51047229 synonymous variant A/C snv 8.0E-06 1
rs11635252 0.925 0.080 15 90528542 upstream gene variant T/C snv 0.88 4
rs1003723 0.925 0.080 19 11113505 non coding transcript exon variant C/A;T snv 4.0E-06; 0.40 2
rs2076310 0.925 0.080 6 33198257 intron variant A/G snv 0.27 0.28 2
rs2230054 0.925 0.080 2 218135587 synonymous variant C/T snv 0.48 0.54 2
rs3769839 0.925 0.080 2 230211910 intron variant T/C snv 0.12 2
rs7731017 0.925 0.080 5 150732056 intron variant T/C snv 8.3E-03 2
rs8004738 0.925 0.080 14 94390577 5 prime UTR variant G/A snv 0.55 2
rs9679162 0.882 0.120 2 31024648 intron variant G/T snv 0.48 4
rs1126580 0.882 0.120 2 218136243 3 prime UTR variant G/A;T snv 3
rs2106261 0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs763569821 0.851 0.160 1 155188197 missense variant T/C snv 1.2E-05 4
rs3219472 0.882 0.160 1 45338378 5 prime UTR variant C/T snv 0.26 3
rs1126579 0.776 0.200 2 218136011 3 prime UTR variant T/C snv 0.62 8
rs3024270 0.776 0.200 11 1996209 non coding transcript exon variant C/G;T snv 0.46; 5.2E-06 8
rs2289278 0.827 0.200 5 111073450 5 prime UTR variant C/G snv 8.7E-02 5
rs3219476 0.882 0.200 1 45336998 intron variant A/C snv 0.58 3
rs2287622 0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 16
rs36053993 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 31
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 16
rs3197999 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 16
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32