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: rs11646011
rs11646011
CDH13
1 1.000 0.040 16 82666121 intron variant T/C snv 0.40 0.010 1.000 1 2016 2016
dbSNP: rs11646643
rs11646643
MMP2
1 1.000 0.040 16 55484965 intron variant A/G snv 0.31 0.010 1.000 1 2015 2015
dbSNP: rs11646849
rs11646849
CDH13 ; LOC101928446
1 1.000 0.040 16 82783646 intron variant G/A snv 0.44 0.010 1.000 1 2016 2016
dbSNP: rs11668247
rs11668247
LOC105372412
1 1.000 0.040 19 43690210 intron variant C/T snv 0.34 0.010 < 0.001 1 2009 2009
dbSNP: rs1176147476
rs1176147476
HMOX1
1 1.000 0.040 22 35386688 missense variant G/T snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs11779254
rs11779254
CSMD1
2 0.925 0.080 8 4391552 intron variant G/C;T snv 0.010 1.000 1 2014 2014
dbSNP: rs11860282
rs11860282
CDH13 ; LOC101928446
1 1.000 0.040 16 82800222 intron variant T/C snv 0.16 0.010 1.000 1 2016 2016
dbSNP: rs11938704
rs11938704
LOC105377462
1 1.000 0.040 4 144522218 intron variant A/C snv 0.23 0.010 1.000 1 2013 2013
dbSNP: rs1202989817
rs1202989817
SOD1 ; LOC102724449
18 0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs1205
rs1205
CRP
46 0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 0.010 1.000 1 2012 2012
dbSNP: rs12068264
rs12068264
CTSS
1 1.000 0.040 1 150754853 intron variant C/T snv 0.34 0.010 1.000 1 2018 2018
dbSNP: rs12150220
rs12150220
NLRP1
14 0.724 0.360 17 5582047 missense variant A/T snv 0.37 0.33 0.010 1.000 1 2019 2019
dbSNP: rs121917864
rs121917864
TLR2
31 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 0.010 < 0.001 1 2009 2009
dbSNP: rs1241561623
rs1241561623
CHRM2 ; LOC349160
1 1.000 0.040 7 137015359 missense variant T/C snv 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs1243160
rs1243160
SERPINA1
1 1.000 0.040 14 94388540 intron variant G/A snv 0.16 0.010 < 0.001 1 2017 2017
dbSNP: rs1243166
rs1243166
SERPINA1
1 1.000 0.040 14 94377481 3 prime UTR variant A/G snv 0.70 0.010 1.000 1 2018 2018
dbSNP: rs12442260
rs12442260
ABHD2
1 1.000 0.040 15 89113236 intron variant T/C snv 0.11 0.010 1.000 1 2015 2015
dbSNP: rs12462372
rs12462372
NLRP4
1 1.000 0.040 19 55862096 missense variant G/A;C snv 8.3E-02 0.010 1.000 1 2019 2019
dbSNP: rs12593229
rs12593229
IREB2
3 1.000 0.040 15 78472948 intron variant T/G snv 0.51 0.010 1.000 1 2012 2012
dbSNP: rs1290569539
rs1290569539
FEV
1 1.000 0.040 2 218981998 missense variant T/C snv 8.1E-06 7.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs12910984
rs12910984
CHRNA3
8 0.827 0.080 15 78599285 intron variant G/A;C;T snv 0.010 1.000 1 2013 2013
dbSNP: rs12922394
rs12922394
CDH13
1 1.000 0.040 16 82638722 intron variant C/T snv 0.11 0.010 1.000 1 2016 2016
dbSNP: rs1295685
rs1295685
IL13 ; TH2LCRR
7 0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 0.010 1.000 1 2010 2010
dbSNP: rs12979270
rs12979270
CYP2B6
1 1.000 0.040 19 41018226 3 prime UTR variant A/C snv 0.21 0.010 1.000 1 2019 2019
dbSNP: rs12979860
rs12979860
IFNL4
84 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2018 2018