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: rs17860508
rs17860508
LOC285626
11 0.752 0.360 5 159333192 intron variant TTAGAG/GC delins 0.010 1.000 1 2010 2010
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: 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: 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: 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: rs3138557
rs3138557
IFNG ; IFNG-AS1
4 0.851 0.080 12 68158711 intron variant CGAG/- 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: rs8179190
rs8179190
IL4 ; LOC105379176
1 1.000 0.040 5 132680584 intron variant AAGCAAGATGGCCTGTTGGGAGGCTACCACAGTAAACCAGGCTAGAGACGATGGTGGCGTGGACAGAATGAAGCAAGATGGCCTGTTGGGAGGCTACCACAGTAAACCAGGCTAGAGATGATGGTGGCGTGGACAGAATG/- delins 0.010 1.000 1 2015 2015
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: 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: 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
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: 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: 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: rs2234237
rs2234237
TREM1
9 0.763 0.280 6 41282728 missense variant T/A snv 0.13 0.12 0.010 1.000 1 2016 2016
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: 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: rs505151
rs505151
PCSK9
18 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.010 1.000 1 2018 2018
dbSNP: rs5743618
rs5743618
TLR1
25 0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 0.010 1.000 1 2016 2016
dbSNP: rs5743810
rs5743810
TLR1 ; TLR6
21 0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 0.010 1.000 1 2016 2016
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