Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs843720
ACYP2 ; LOC105374610
0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs2615787 1.000 0.120 8 6953627 upstream gene variant T/G snv 0.41 1
rs7389
TREH ; PHLDB1
1.000 0.120 11 118657756 3 prime UTR variant T/G snv 0.32 1
rs3218896
IL1R2
0.807 0.160 2 102015190 intron variant T/C;G snv 6
rs7522061
FCRL3
0.882 0.320 1 157698600 missense variant T/C;G snv 0.45 0.51 4
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs4833095
TLR1
0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 15
rs372883
BACH1
0.827 0.360 21 29345416 3 prime UTR variant T/C snv 0.53 5
rs8190315
BID
0.851 0.240 22 17743998 missense variant T/C snv 2.4E-02 3.6E-02 5
rs11574637
ITGAX
0.882 0.200 16 31357553 missense variant T/C snv 0.21 3
rs11150619
ITGAX
0.925 0.160 16 31365528 intron variant T/C snv 0.29 2
rs2738058 0.925 0.160 8 6964095 upstream gene variant T/C snv 0.57 2
rs7190997
ITGAX
1.000 0.120 16 31356857 intron variant T/C snv 0.52 2
rs1055901
SERPINB7
1.000 0.120 18 63805221 3 prime UTR variant T/C snv 0.61 1
rs1369270 1.000 0.120 2 153179546 intron variant T/C snv 1
rs140433921
SLC3A1
1.000 0.120 2 44286102 start lost T/C snv 2.0E-05 5.6E-05 1
rs2188404
VPS50
1.000 0.120 7 93314448 intron variant T/C snv 0.30 1
rs637571
FOSL1
1.000 0.120 11 65896875 synonymous variant T/C snv 0.51 0.50 1
rs6984215 1.000 0.120 8 7027356 downstream gene variant T/C snv 0.30 1