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: 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: rs2032582
rs2032582
ABCB1
97 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2017 2017
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: 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: 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: 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: 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: 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: 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: rs2069728
rs2069728
IFNG-AS1
2 0.925 0.120 12 68154004 intron variant C/T snv 0.13 0.010 1.000 1 2015 2015
dbSNP: rs2069718
rs2069718
IFNG ; IFNG-AS1
14 0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 0.010 1.000 1 2015 2015
dbSNP: rs2069727
rs2069727
IFNG ; IFNG-AS1
9 0.763 0.320 12 68154443 intron variant T/A;C snv 0.010 1.000 1 2015 2015
dbSNP: rs3138557
rs3138557
IFNG ; IFNG-AS1
4 0.851 0.080 12 68158711 intron variant CGAG/- delins 0.010 1.000 1 2015 2015
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: 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: rs708567
rs708567
IL17RC
6 0.807 0.200 3 9918386 missense variant C/T snv 0.46 0.51 0.010 1.000 1 2012 2012
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: 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: rs8179190
rs8179190
IL4 ; LOC105379176
1 1.000 0.040 5 132680584 intron variant AAGCAAGATGGCCTGTTGGGAGGCTACCACAGTAAACCAGGCTAGAGACGATGGTGGCGTGGACAGAATGAAGCAAGATGGCCTGTTGGGAGGCTACCACAGTAAACCAGGCTAGAGATGATGGTGGCGTGGACAGAATG/- delins 0.010 1.000 1 2015 2015
dbSNP: rs7291467
rs7291467
LGALS2
4 0.851 0.160 22 37576621 intron variant G/A snv 0.49 0.010 1.000 1 2010 2010
dbSNP: rs17860508
rs17860508
LOC285626
11 0.752 0.360 5 159333192 intron variant TTAGAG/GC delins 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