Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs174549
FADS2 ; FADS1
0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 12
rs2239633
CEBPE
0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 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
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs218265 4 54542832 intergenic variant T/C snv 0.21 10
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 9
rs150813342
GFI1B
9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 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
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 9
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs1420101
IL1RL1 ; IL18R1
0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 8
rs2228467
CYP8B1 ; KRBOX1 ; ACKR2
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02 8
rs34210653
ALOX15
0.807 0.280 17 4632019 missense variant G/A snv 2.7E-02 1.7E-02 8
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs34599082
ACKR1 ; CADM3-AS1
1 159205704 missense variant C/T snv 1.1E-02 9.9E-03 8