Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1569686 0.752 0.400 20 32779273 intron variant G/A;C;T snv 15
rs1805010 0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 12
rs9261290 0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs3130618 0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 7
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 6
rs3132685 0.807 0.320 6 29978172 intron variant G/A;T snv 6
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs204990 0.851 0.280 6 32193653 intron variant C/A;T snv 4
rs2844659 0.851 0.280 6 30856755 intergenic variant C/G;T snv 4
rs1422673 0.925 0.160 5 151059427 intron variant C/G;T snv 2
rs2071591 0.925 0.160 6 31548022 intron variant G/A;C snv 2
rs2737713 1.000 0.120 1 236537507 missense variant T/A snv 2
rs887464 0.925 0.200 6 31178143 intron variant C/A;T snv 2
rs11466316 1.000 0.120 19 41353431 5 prime UTR variant G/A;T snv 1
rs150881176 1.000 0.120 6 29979963 downstream gene variant T/C snv 1
rs8058696 1.000 0.120 16 16185012 synonymous variant G/C;T snv 0.42 1
rs9963862 1.000 0.120 18 23007948 intron variant G/A;C snv 1
rs564353179 1.000 0.120 2 178780121 missense variant C/G snv 9.6E-05 9.1E-05 1
rs11575936 0.851 0.200 6 137219288 missense variant C/T snv 1.3E-03 4.1E-04 4
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs7749323 0.925 0.200 6 137909252 intergenic variant G/A snv 3.3E-02 2
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs1235162 0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs7775397 0.790 0.400 6 32293475 missense variant T/G snv 6.0E-02 6.4E-02 7