Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs447372
DKK2
0.882 0.080 4 106932839 intron variant G/A snv 0.48 3
rs4262299
ANGPT1
0.882 0.080 8 107330035 intron variant A/C;T snv 3
rs1654701
ANGPT1
0.882 0.080 8 107366717 intron variant G/A snv 0.52 3
rs793544 0.882 0.080 3 107368152 intron variant T/C snv 0.35 3
rs807185
ATG4A
0.882 0.080 X 108097488 intron variant A/T snv 3
rs1326656542
LIG4
0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06 10
rs1805388
LIG4
0.790 0.120 13 108211243 missense variant G/A snv 0.18 0.16 11
rs189037
ATM ; NPAT
0.689 0.400 11 108223106 5 prime UTR variant G/A snv 0.49 22
rs664677
ATM
0.807 0.160 11 108272455 intron variant C/A;T snv 0.65 8
rs624366
ATM
0.827 0.120 11 108283370 intron variant G/C snv 0.52 6
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs1878022
CMKLR1
0.851 0.080 12 108305255 intron variant C/T snv 0.70 4
rs11212592
ATM ; C11orf65
0.882 0.080 11 108348120 intron variant A/G snv 0.16 3
rs664143
C11orf65 ; ATM
0.807 0.160 11 108354934 3 prime UTR variant A/G;T snv 8
rs652311
C11orf65 ; ATM
0.882 0.080 11 108369342 intron variant G/A snv 0.54 3
rs4978754
ELP1
0.851 0.080 9 108884801 intron variant T/C snv 0.92 4
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs536289169
GSTM1 ; GSTM2
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 13
rs7483
GSTM3 ; GSTM5
0.742 0.320 1 109737079 missense variant C/T snv 4.0E-06; 0.35 0.26 11
rs774352237
TCHP
0.882 0.080 12 109908873 missense variant G/A snv 3.2E-05 2.1E-05 4
rs770178049
TCHP
0.882 0.080 12 109912997 missense variant G/A;C snv 4.0E-06; 4.0E-06 3
rs1436919825
EGF
0.882 0.080 4 109976175 missense variant G/A snv 3
rs465646
REV3L ; MFSD4B
0.882 0.080 6 111299555 3 prime UTR variant G/A snv 0.80 3
rs459809
REV3L ; MFSD4B
0.882 0.080 6 111331964 intron variant T/C snv 0.71 3
rs1002481
REV3L ; MFSD4B
0.882 0.080 6 111390819 intron variant T/A;G snv 3