Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs34568801
PLA2G2A
1.000 0.040 1 19975708 missense variant C/T snv 4.6E-03 4.3E-03 1
rs516651
EGLN1
1.000 0.040 1 231406910 intron variant C/T snv 0.15 1
rs672961
LRRC7
1.000 0.040 1 70101505 intron variant C/G snv 0.99 1
rs315952
IL1RN
0.763 0.400 2 113132727 missense variant T/A;C snv 4.0E-06; 0.31 10
rs1130866
SFTPB
0.827 0.160 2 85666618 missense variant G/A;C snv 0.50 9
rs13402990
C2orf42 ; TIA1
1.000 0.040 2 70231632 intron variant A/T snv 9.7E-03 1
rs2592178
C2orf42 ; TIA1
1.000 0.040 2 70245350 intron variant G/A snv 0.27 1
rs7744
MYD88
0.827 0.160 3 38142530 3 prime UTR variant A/G snv 0.13 5
rs121434431
TLR3
0.851 0.080 4 186083346 missense variant C/T snv 4.1E-04 5.2E-04 4
rs3774934
NFKB1
0.851 0.080 4 102506319 intron variant A/C;G;T snv 4
rs7692976
EGF
1.000 0.040 4 109990411 intron variant A/G;T snv 2
rs2298991
EGF
1.000 0.040 4 109970856 intron variant T/A;G snv 1
rs4698803
EGF
1.000 0.040 4 109993271 missense variant A/G;T snv 0.85 1
rs6533485
EGF
1.000 0.040 4 110006407 intron variant G/C snv 0.61 1
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 5
rs761495176
NR3C1
0.882 0.080 5 143400263 missense variant T/C snv 1.7E-05 3
rs832582
MAP3K1
0.925 0.080 5 56881916 missense variant G/A snv 0.76 0.78 2
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1805018
PLA2G7
0.827 0.200 6 46711566 missense variant A/G snv 6.8E-02 0.10 6