Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs2066845
NOD2
0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs2249825
HMGB1
0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs1043210477
GPX1
0.701 0.520 3 49358250 missense variant G/A snv 19
rs747126003
IL6-AS1 ; IL6
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06 18
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs7096206
MBL2
0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs5743551
TLR1
0.742 0.240 4 38806033 intron variant T/A;C snv 12
rs17281995
CD86
0.763 0.360 3 122120794 3 prime UTR variant G/A;C snv 11
rs11568821
LOC105373977 ; PDCD1
0.827 0.200 2 241851760 intron variant C/G;T snv 10
rs414171
MAPKAPK3 ; CISH
0.790 0.200 3 50612068 5 prime UTR variant A/G;T snv 9
rs121918094
TTR
0.827 0.280 18 31592921 missense variant T/C snv 8
rs212388
LOC112267968 ; LOC105378083
0.827 0.240 6 159069404 intron variant C/G;T snv 8
rs4358188
BPI
0.827 0.160 20 38318446 missense variant G/A;C snv 0.46 7
rs1799768
SERPINE1
0.807 0.360 7 101126425 upstream gene variant -/A;C ins 6
rs2857656
CCL2
0.851 0.120 17 34254988 upstream gene variant G/A;C snv 5
rs6586282
CBS
0.882 0.080 21 43058387 intron variant C/T snv 5