Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7922612 0.752 0.080 10 94051682 intron variant C/T snv 0.39 14
rs10484761 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 7
rs2274224 0.882 0.080 10 94279840 missense variant G/A;C snv 8.8E-05; 0.44 6
rs10509670 0.851 0.080 10 94308190 intron variant A/G snv 0.30 5
rs13016963 0.851 0.080 2 201298088 intron variant A/G snv 0.59 5
rs2014300 0.851 0.080 21 34985564 intron variant A/G;T snv 0.75 5
rs2228059 0.882 0.080 10 5960405 missense variant T/G snv 0.51 0.55 5
rs4462560 0.851 0.080 15 75355623 3 prime UTR variant G/C snv 0.64 5
rs756826500 0.925 0.080 19 45413705 missense variant G/A snv 4.0E-06 5
rs11473
BSG
0.882 0.080 19 582982 3 prime UTR variant C/A;T snv 4
rs11548103 0.882 0.080 1 153615864 splice region variant C/T snv 0.40 0.39 4
rs145188037 0.925 0.080 7 45914866 missense variant G/A snv 1.1E-02 9.9E-03 4
rs1595066 0.882 0.080 2 211377000 3 prime UTR variant C/T snv 0.28 4
rs16845990 0.882 0.080 2 211378286 3 prime UTR variant T/A;C snv 4
rs2244438 0.882 0.080 2 201387816 missense variant G/A;T snv 0.29; 4.0E-06 4
rs353163 0.882 0.080 4 67919056 missense variant T/A;C;G snv 0.67 4
rs3738894 0.882 0.080 2 46187030 3 prime UTR variant G/A snv 1.1E-02 4
rs1014867 0.925 0.080 4 125491736 missense variant C/T snv 4.9E-02 4.9E-02 3
rs1039808 0.925 0.080 4 125318831 missense variant C/G;T snv 4.0E-06; 0.41 3
rs12508222 0.925 0.080 4 125449492 missense variant G/A;T snv 4.3E-02; 2.0E-05 3
rs1364898025
ATM
0.925 0.080 11 108227656 missense variant G/A snv 3
rs1567047 0.925 0.080 4 125451587 missense variant G/A snv 0.27 0.22 3
rs2320615 0.925 0.080 4 163148797 intron variant A/G snv 0.78 3
rs312986 0.925 0.080 18 1898710 intron variant A/G;T snv 3
rs31564
IL9
0.925 0.080 5 135894564 intron variant G/A;T snv 3