Source: CURATED ×
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: rs1295686
rs1295686
IL13 ; TH2LCRR
3 0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 0.800 1.000 2 2013 2015
dbSNP: rs13015714
rs13015714
IL18R1
2 0.882 0.200 2 102355405 intron variant G/T snv 0.77 0.800 1.000 2 2012 2015
dbSNP: rs2897442
rs2897442
KIF3A
1 0.925 0.120 5 132713335 intron variant C/A;T snv 0.820 1.000 2 2011 2015
dbSNP: rs6010620
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
4 0.701 0.360 20 63678486 intron variant A/C;G snv 0.810 0.667 2 2011 2015
dbSNP: rs10067777
rs10067777
TMEM232
1 1.000 0.120 5 110490595 intron variant A/G snv 7.4E-02 0.700 1.000 1 2011 2011
dbSNP: rs10199605
rs10199605
LINC00299
1 1.000 0.120 2 8354967 intron variant G/A snv 0.26 0.700 1.000 1 2015 2015
dbSNP: rs10445308
rs10445308
IKZF3
5 0.851 0.240 17 39781794 intron variant C/T snv 0.38 0.700 1.000 1 2015 2015
dbSNP: rs10791824
rs10791824
OVOL1 ; OVOL1-AS1
3 0.882 0.160 11 65791795 intron variant A/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs10995251
rs10995251
ZNF365 ; LOC105378327
1 1.000 0.120 10 62638706 intron variant C/T snv 0.29 0.800 1.000 1 2012 2012
dbSNP: rs11204971
rs11204971
FLG-AS1
1 0.925 0.120 1 152286602 intron variant A/G snv 0.15 0.710 1.000 1 2011 2012
dbSNP: rs12153855
rs12153855
TNXB
10 0.776 0.320 6 32107027 intron variant T/C snv 0.11 0.800 1.000 1 2013 2013
dbSNP: rs12188917
rs12188917
IL13 ; TH2LCRR
1 1.000 0.120 5 132655393 intron variant T/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs12198173
rs12198173
TNXB
9 0.827 0.240 6 32059031 intron variant G/A snv 0.10 0.700 1.000 1 2013 2013
dbSNP: rs13199524
rs13199524
TNXB
9 0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 0.700 1.000 1 2013 2013
dbSNP: rs13360927
rs13360927
TMEM232
1 0.882 0.160 5 110700055 intron variant A/G snv 9.3E-02 0.710 1.000 1 2011 2012
dbSNP: rs13361382
rs13361382
TMEM232
1 0.882 0.160 5 110713253 intron variant G/A snv 9.3E-02 0.710 1.000 1 2011 2012
dbSNP: rs1444418
rs1444418 		1 1.000 0.120 10 62800710 intron variant A/G snv 0.22 0.800 1.000 1 2012 2012
dbSNP: rs1665050
rs1665050
RNF111
1 1.000 0.120 15 59001406 intron variant A/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs17881320
rs17881320
STAT3
1 1.000 0.120 17 42333221 intron variant G/A;T snv 6.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs2041733
rs2041733
CLEC16A ; LOC105371081
1 1.000 0.120 16 11135732 intron variant T/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs2059876
rs2059876
CHST8
2 0.925 0.120 19 33639430 intron variant C/T snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs2143950
rs2143950
PPP2R3C ; FAM177A1 ; LOC101927178
1 1.000 0.120 14 35103151 intron variant C/T snv 0.17 0.700 1.000 1 2015 2015
dbSNP: rs2158177
rs2158177
TH2LCRR
4 0.925 0.120 5 132648366 intron variant A/G snv 0.18 0.710 1.000 1 2013 2017
dbSNP: rs2393903
rs2393903
ZNF365
1 1.000 0.120 10 62620576 intron variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs2533291
rs2533291
PTPRN2
2 0.925 0.120 7 157712962 intron variant C/T snv 0.12 0.700 1.000 1 2015 2015