Source: GWASDB ×
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: rs11071559
rs11071559
RORA
1 0.925 0.080 15 60777789 intron variant C/T snv 0.23 0.820 1.000 3 2010 2019
dbSNP: rs1588265
rs1588265
PDE4D
1 1.000 0.080 5 60073967 intron variant A/G;T snv 0.800 1.000 3 2009 2011
dbSNP: rs744910
rs744910
SMAD3
1 1.000 0.080 15 67154447 intron variant G/A;T snv 0.810 1.000 3 2010 2012
dbSNP: rs9273349
rs9273349
HLA-DQB1-AS1
1 0.827 0.200 6 32658092 upstream gene variant T/C;G snv 0.810 1.000 3 2010 2012
dbSNP: rs11778371
rs11778371
CHRNA2
1 1.000 0.080 8 27462388 intron variant C/T snv 4.0E-02 0.700 1.000 2 2009 2010
dbSNP: rs12150079
rs12150079
ZPBP2
1 0.807 0.280 17 39869164 intron variant G/A snv 0.24 0.700 1.000 2 2010 2011
dbSNP: rs1810132
rs1810132
ERBB2
1 1.000 0.080 17 39709752 intron variant C/T snv 0.64 0.700 1.000 2 2010 2011
dbSNP: rs2271308
rs2271308
STARD3
1 1.000 0.080 17 39661229 non coding transcript exon variant T/C snv 0.61 0.700 1.000 2 2010 2011
dbSNP: rs2548659
rs2548659
PDE4D
1 1.000 0.080 5 60088059 intron variant A/G snv 0.28 0.700 1.000 2 2009 2010
dbSNP: rs983280
rs983280
PDE4D
1 1.000 0.080 5 60149310 intron variant C/T snv 0.68 0.700 1.000 2 2009 2010
dbSNP: rs1007654
rs1007654
GSDMA
1 1.000 0.080 17 39955101 intron variant A/G snv 0.69 0.700 1.000 1 2010 2010
dbSNP: rs10204137
rs10204137
IL18R1 ; IL1RL1
1 0.925 0.160 2 102351752 missense variant A/G;T snv 0.34 0.700 1.000 1 2010 2010
dbSNP: rs10211025
rs10211025 		1 1.000 0.080 2 41801493 intergenic variant A/G snv 0.12 0.700 1.000 1 2014 2014
dbSNP: rs10508372
rs10508372 		1 1.000 0.080 10 8930055 intergenic variant G/A snv 0.14 0.800 1.000 1 2011 2011
dbSNP: rs1058808
rs1058808
ERBB2
1 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 0.710 1.000 1 2011 2013
dbSNP: rs1061477
rs1061477
KLK3
1 1.000 0.080 19 50856840 intron variant T/C snv 0.42 0.700 1.000 1 2012 2012
dbSNP: rs10800812
rs10800812 		1 1.000 0.080 1 202086810 intergenic variant A/G snv 0.77 0.700 1.000 1 2000 2000
dbSNP: rs1101999
rs1101999
PYHIN1
1 1.000 0.080 1 158962765 intron variant C/T snv 0.92 0.800 1.000 1 2011 2011
dbSNP: rs11048311
rs11048311 		1 1.000 0.080 12 25869205 downstream gene variant A/C snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs11048317
rs11048317
MIR4302
1 1.000 0.080 12 25875474 upstream gene variant T/G snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs11078936
rs11078936
MED24
1 1.000 0.080 17 40041661 intron variant T/C snv 0.29 0.700 1.000 1 2010 2010
dbSNP: rs11214966
rs11214966
LOC101928940
1 1.000 0.080 11 114360533 intron variant T/C snv 0.13 0.800 1.000 1 2011 2011
dbSNP: rs11242168
rs11242168
FSTL4
1 1.000 0.080 5 133667444 intergenic variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs11252191
rs11252191
LINC02660
1 1.000 0.080 10 3921969 intron variant C/A;G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs113612868
rs113612868
TCAP
1 1.000 0.080 17 39665182 upstream gene variant -/T ins 0.700 1.000 1 2010 2010