Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 14
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13
rs7296503
PDZRN4
12 41306962 intron variant C/T snv 0.57 13
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03 13
rs9917425
OTOR
20 16755400 intron variant G/T snv 0.16 13
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs2179593
TOX2
0.790 0.080 20 44031646 intron variant C/A snv 0.71 11
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs76428106
FLT3
0.851 0.040 13 28029870 intron variant T/C;G snv 10
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 9
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 9
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs2393791
HNF1A
0.925 0.160 12 120986153 intron variant C/T snv 0.62 8
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26 7