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
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 24
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs696
NFKBIA
0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 22
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
rs2516839
USF1
0.732 0.320 1 161043331 5 prime UTR variant C/T snv 0.49 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
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 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
rs174549
FADS2 ; FADS1
0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 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
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11