Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 14
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 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
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 9
rs2954031 8 125479491 intron variant G/T snv 0.42 9
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs9532434
COG6
0.807 0.120 13 39781776 intron variant T/A;C snv 8
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26 7