Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs2230926 0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs2839698 0.662 0.520 11 1997623 non coding transcript exon variant G/A snv 0.41 25
rs10516487 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs2205960 0.763 0.400 1 173222336 intergenic variant G/A;T snv 9
rs7812879 0.807 0.320 8 11482672 upstream gene variant T/A;C snv 6
rs13447 0.882 0.200 7 75166663 non coding transcript exon variant T/A;C snv 1.9E-02 4
rs201802880 0.882 0.200 7 74779296 missense variant G/A snv 1.1E-03 4
rs4522865 0.882 0.240 4 101794731 intron variant G/A;T snv 4
rs485497 0.925 0.200 3 160001345 intron variant A/C;G snv 2
rs1376314937 1.000 0.200 9 114361709 missense variant G/A snv 4.0E-06 1
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs387907272 0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs117026326 0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs11575837 1.000 0.200 6 31592893 5 prime UTR variant C/T snv 2.4E-02 2
rs3135945 1.000 0.200 3 48467567 synonymous variant G/A snv 9.4E-03 4.0E-02 2
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs2070197 0.827 0.280 7 128948946 3 prime UTR variant T/C snv 9.0E-02 6
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs8177374 0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs12583006 0.807 0.320 13 108285104 intron variant T/A snv 0.21 8
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs3792783 0.882 0.280 5 151076171 intron variant A/G snv 0.25 3