Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs7708392
TNIP1
0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs1391441
TET2-AS1 ; TET2
0.763 0.240 4 105207603 intron variant G/A snv 0.70 11
rs3824662
GATA3
0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs4958881
TNIP1
0.827 0.280 5 151070675 intron variant T/C snv 0.21 7
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 7
rs292001
C1QA
0.807 0.320 1 22638465 intron variant G/A snv 0.54 6
rs11981433
PON2
0.882 0.240 7 95425028 intron variant T/C;G snv 4
rs4664308
LOC105373717 ; PLA2R1
0.851 0.160 2 160060986 intron variant A/G snv 0.30 4
rs11203368
PADI4
0.925 0.200 1 17340013 intron variant C/T snv 0.57 3
rs434082
SLC8A1
0.925 0.160 2 40257934 intron variant C/T snv 0.14 3
rs8091180
NFATC1
1.000 0.160 18 79404243 intron variant G/A snv 0.46 3
rs11057864
SCARB1
0.925 0.160 12 124851404 intron variant C/A snv 6.5E-02 2
rs1108131
CAMK1D
0.925 0.160 10 12455748 intron variant T/C snv 0.28 2
rs11893826
SLC8A1
0.925 0.160 2 40337507 intron variant G/A snv 0.27 2
rs1364989 0.925 0.160 4 54145602 intron variant T/C snv 0.73 2
rs1635564
PADI4
0.925 0.160 1 17357031 intron variant T/A;G snv 2
rs274068
SLC5A11
0.925 0.160 16 24887651 intron variant C/A snv 0.74 2
rs3792192
PLA2R1
0.925 0.160 2 160030364 intron variant G/A snv 0.35 2
rs7773456 0.925 0.160 6 19823007 intron variant T/G snv 0.35 2
rs8012283
NIN
0.925 0.160 14 50767442 intron variant A/G snv 0.23 2
rs2157257
MYH9
1.000 0.160 22 36312293 intron variant A/G snv 0.52 1
rs2271100
AGA
1.000 0.160 4 177438525 intron variant T/C snv 0.19 1