Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs4986938 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs41423247 0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs334558 0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs1805054 0.708 0.200 1 19666020 synonymous variant C/T snv 0.15; 8.0E-06 0.16 17
rs2230912 0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs1043307 0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs3219151 0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs749437638 0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 14
rs2227631 0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 13
rs2072446 0.776 0.160 17 49510457 missense variant C/T snv 5.2E-02 4.1E-02 11