Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.407 0.786 7 140753336 missense variant snp 4.0E-06 267
rs397507444 0.457 0.714 1 11794407 missense variant T/G snp 169
rs1799945 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 152
rs25487 0.485 0.679 19 43551574 missense variant T/C snp 0.68 0.72 119
rs1799782 0.523 0.607 19 43553422 stop gained G/A snp 9.5E-02 7.1E-02 84
rs13181 0.525 0.536 19 45351661 stop gained T/A,G snp 4.0E-06; 0.32 0.32 82
rs4880 0.536 0.643 6 159692840 missense variant A/G snp 0.48 0.47 81
rs1052133 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 77
rs671 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 61
rs7903146 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 59
rs17879961 0.615 0.321 22 28725099 missense variant A/C,G snp 4.1E-03 1.1E-02 33
rs1544410
VDR
0.626 0.607 12 47846052 intron variant C/A,G,T snp 0.34 32
rs2228570
VDR
0.622 0.607 12 47879112 start lost A/C,G,T snp 0.63 0.65 32
rs1045485 0.652 0.393 2 201284866 missense variant G/A,C,T snp 4.0E-06; 9.0E-02 3.2E-05; 9.8E-02 26
rs11571833 0.652 0.250 13 32398489 stop gained A/T snp 6.6E-03 5.4E-03 23
rs1801516
ATM
0.715 0.214 11 108304735 missense variant G/A snp 0.11 0.11 15
rs3218536 0.769 0.179 7 152648922 missense variant C/G,T snp 4.0E-06; 6.4E-02 4.9E-02 9