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: rs10800812
rs10800812 		1 1.000 0.080 1 202086810 intergenic variant A/G snv 0.77 0.700 1.000 1 2000 2000
dbSNP: rs1229598
rs1229598 		1 1.000 0.080 18 56267556 regulatory region variant A/C;G;T snv 0.700 1.000 1 2000 2000
dbSNP: rs17064520
rs17064520
NEDD4L
1 1.000 0.080 18 58242398 intron variant C/T snv 0.19 0.700 1.000 1 2000 2000
dbSNP: rs2153101
rs2153101 		1 1.000 0.080 1 203199346 intergenic variant A/T snv 0.84 0.700 1.000 1 2000 2000
dbSNP: rs2538026
rs2538026 		1 1.000 0.080 18 56261410 intergenic variant A/C;G snv 0.700 1.000 1 2000 2000
dbSNP: rs4436440
rs4436440 		1 1.000 0.080 1 202082885 TF binding site variant T/A snv 0.80 0.700 1.000 1 2000 2000
dbSNP: rs4950929
rs4950929 		1 1.000 0.080 1 203190998 upstream gene variant G/T snv 0.84 0.700 1.000 1 2000 2000
dbSNP: rs545854
rs545854 		2 0.882 0.160 8 10002570 intron variant G/C snv 0.85 0.700 1.000 1 2000 2000
dbSNP: rs946263
rs946263 		1 1.000 0.080 1 203196253 intergenic variant G/A snv 0.86 0.700 1.000 1 2000 2000
dbSNP: rs7216389
rs7216389
GSDMB
3 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.900 0.889 4 2007 2018
dbSNP: rs2305480
rs2305480
GSDMB
7 0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 0.860 0.900 4 2008 2018
dbSNP: rs12603332
rs12603332
ORMDL3 ; LRRC3C ; LOC112268187
3 0.807 0.200 17 39926554 5 prime UTR variant T/C snv 0.49 0.730 1.000 1 2008 2017
dbSNP: rs4795400
rs4795400
GSDMB
3 0.925 0.080 17 39910767 intron variant C/T snv 0.36 0.710 1.000 1 2008 2011
dbSNP: rs8069176
rs8069176 		3 0.882 0.080 17 39900944 downstream gene variant G/A;T snv 0.740 1.000 1 2008 2018
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: 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: 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: rs1544791
rs1544791
PDE4D
1 1.000 0.080 5 60143255 intron variant T/A;C snv 0.710 1.000 1 2009 2016
dbSNP: rs3894194
rs3894194
GSDMA
2 0.882 0.120 17 39965740 missense variant G/A snv 0.46 0.41 0.810 1.000 4 2010 2014
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: rs1295686
rs1295686
IL13 ; TH2LCRR
2 0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 0.840 1.000 3 2010 2018
dbSNP: rs1342326
rs1342326 		2 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 0.840 1.000 3 2010 2020
dbSNP: rs1837253
rs1837253 		2 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 0.840 0.929 3 2010 2019
dbSNP: rs2073643
rs2073643
SLC22A5
4 1.000 0.080 5 132387596 intron variant T/C snv 0.46 0.800 1.000 3 2010 2012