Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12212067
rs12212067
FOXO3
20 0.716 0.320 6 108659993 intron variant T/G snv 0.14 0.020 0.500 2 2013 2015
dbSNP: rs1463502008
rs1463502008
PRH1 ; PRH2 ; PRR4 ; PRH1-PRR4
2 0.925 0.040 12 10930275 missense variant G/C snv 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs4986790
rs4986790
TLR4
223 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.020 0.500 2 2006 2017
dbSNP: rs4986791
rs4986791
TLR4
182 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2006 2006
dbSNP: rs8177374
rs8177374
TIRAP
22 0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 0.010 1.000 1 2016 2016
dbSNP: rs1881457
rs1881457
IL13 ; TH2LCRR
9 0.790 0.280 5 132656717 intron variant A/C snv 0.21 0.010 1.000 1 2009 2009
dbSNP: rs1800925
rs1800925
IL13 ; TH2LCRR
37 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs2070874
rs2070874
IL4
27 0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 0.010 1.000 1 2015 2015
dbSNP: rs2243267
rs2243267
IL4
3 0.882 0.160 5 132678194 intron variant G/A;C snv 0.010 1.000 1 2009 2009
dbSNP: rs2243268
rs2243268
IL4
3 0.882 0.040 5 132678271 intron variant A/C snv 0.23 0.010 1.000 1 2009 2009
dbSNP: rs8179190
rs8179190
IL4 ; LOC105379176
1 1.000 0.040 5 132680584 intron variant AAGCAAGATGGCCTGTTGGGAGGCTACCACAGTAAACCAGGCTAGAGACGATGGTGGCGTGGACAGAATGAAGCAAGATGGCCTGTTGGGAGGCTACCACAGTAAACCAGGCTAGAGATGATGGTGGCGTGGACAGAATG/- delins 0.010 1.000 1 2015 2015
dbSNP: rs2243282
rs2243282
IL4 ; LOC105379176
1 1.000 0.040 5 132680862 intron variant C/A;T snv 0.010 1.000 1 2009 2009
dbSNP: rs5744454
rs5744454
CD14 ; TMCO6
1 1.000 0.040 5 140633982 upstream gene variant T/C;G snv 0.010 1.000 1 2018 2018
dbSNP: rs76723693
rs76723693
G6PD
3 0.882 0.160 X 154533025 missense variant A/G snv 5.3E-04 1.5E-03 0.010 1.000 1 2014 2014
dbSNP: rs17860508
rs17860508
LOC285626
11 0.752 0.360 5 159333192 intron variant TTAGAG/GC delins 0.010 1.000 1 2010 2010
dbSNP: rs762513613
rs762513613
FCGR2C
11 0.752 0.280 1 161591315 missense variant A/G snv 4.2E-06 7.4E-06 0.010 1.000 1 2010 2010
dbSNP: rs34383331
rs34383331
MIF-AS1
3 0.882 0.040 22 23895892 non coding transcript exon variant T/A snv 0.19 0.18 0.010 1.000 1 2013 2013
dbSNP: rs9624472
rs9624472
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
2 0.925 0.040 22 24438763 splice region variant A/G snv 0.10 0.010 1.000 1 2010 2010
dbSNP: rs9282801
rs9282801
NOS2
1 1.000 0.040 17 27769447 intron variant C/A snv 0.32 0.010 1.000 1 2015 2015
dbSNP: rs1799964
rs1799964
LTA ; TNF ; LOC100287329
47 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2007 2007
dbSNP: rs1800630
rs1800630
LTA ; TNF ; LOC100287329
17 0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 0.010 1.000 1 2007 2007
dbSNP: rs1799724
rs1799724
LTA ; TNF
47 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2007 2007
dbSNP: rs1046089
rs1046089
PRRC2A
4 0.882 0.200 6 31635190 missense variant G/A snv 0.36 0.40 0.010 1.000 1 2009 2009
dbSNP: rs2257167
rs2257167
IFNAR1
7 0.807 0.200 21 33343393 missense variant G/C snv 0.18 0.16 0.010 1.000 1 2003 2003
dbSNP: rs867186
rs867186
PROCR ; MMP24-AS1-EDEM2
15 0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 0.020 1.000 2 2014 2016