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: 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: 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: 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: rs993269089
rs993269089
ACOT7
1 1.000 0.040 1 6385564 missense variant A/C;T snv 4.0E-06 0.010 < 0.001 1 2014 2014
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: 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: rs1128503
rs1128503
ABCB1
64 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 0.010 1.000 1 2017 2017
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: 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: 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: 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: 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