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: rs2230804
rs2230804
CHUK
1 10 100218126 missense variant C/T snv 0.47 0.57 0.010 1.000 1 2014 2014
dbSNP: rs17639215
rs17639215
IL18R1 ; IL1RL1
1 2 102336984 intron variant G/A snv 9.7E-02 0.010 1.000 1 2014 2014
dbSNP: rs6967330
rs6967330
CDHR3
8 0.827 0.120 7 106018005 missense variant G/A snv 0.19 0.21 0.040 1.000 4 2015 2020
dbSNP: rs408223
rs408223
CDHR3
2 1.000 0.080 7 106021578 intron variant C/G snv 0.27 0.010 1.000 1 2020 2020
dbSNP: rs121912633
rs121912633
TRPV4
10 0.790 0.240 12 109792396 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs3742030
rs3742030
TRPV4
4 0.925 0.080 12 109814742 missense variant G/A;C snv 3.7E-02 0.010 < 0.001 1 2010 2010
dbSNP: rs4986790
rs4986790
TLR4
223 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs1217691063
rs1217691063
MTHFR
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.010 < 0.001 1 2012 2012
dbSNP: rs146855738
rs146855738
HNF1A ; C12orf43
2 1.000 0.080 12 121001145 missense variant G/A;C snv 3.6E-05; 4.0E-06; 8.0E-06 5.6E-05 0.010 1.000 1 2008 2008
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 2013 2013
dbSNP: rs20541
rs20541
IL13 ; TH2LCRR
52 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 0.020 1.000 2 2009 2013
dbSNP: rs848
rs848
IL13 ; TH2LCRR
8 0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 0.010 1.000 1 2013 2013
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 2017 2017
dbSNP: rs2569191
rs2569191
CD14 ; TMCO6
2 1.000 0.080 5 140634318 upstream gene variant C/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs2915863
rs2915863
CD14 ; TMCO6
3 0.925 0.160 5 140634792 upstream gene variant C/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs1042713
rs1042713
ADRB2
63 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 < 0.001 1 2012 2012
dbSNP: rs3775291
rs3775291
TLR3
51 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 0.010 1.000 1 2012 2012
dbSNP: rs9290936
rs9290936
IL1RAP
1 3 190534846 intron variant G/T snv 0.20 0.010 1.000 1 2014 2014
dbSNP: rs10513854
rs10513854
IL1RAP
1 3 190588085 intron variant C/T snv 0.18 0.010 1.000 1 2014 2014
dbSNP: rs3024492
rs3024492
IL10 ; IL19
1 1 206770767 5 prime UTR variant T/A snv 0.17 0.010 1.000 1 2013 2013
dbSNP: rs1800896
rs1800896
IL10 ; IL19
113 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2017 2017
dbSNP: rs1800890
rs1800890
IL19
29 0.658 0.400 1 206776020 intron variant A/T snv 0.32 0.010 1.000 1 2017 2017
dbSNP: rs2981573
rs2981573
IL20
4 0.882 0.160 1 206867232 intron variant G/A snv 0.77 0.010 1.000 1 2011 2011
dbSNP: rs1051740
rs1051740
EPHX1
56 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2011 2011
dbSNP: rs2234922
rs2234922
EPHX1
42 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.010 1.000 1 2011 2011