Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 23
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 20
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 15
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 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
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
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 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
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 8