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: rs113612868
rs113612868
TCAP
1 1.000 0.080 17 39665182 upstream gene variant -/T ins 0.700 1.000 1 2010 2010
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: rs10045431
rs10045431 		3 0.851 0.240 5 159387525 intron variant A/C snv 0.78 0.700 1.000 1 2011 2011
dbSNP: rs1054609
rs1054609
ZPBP2
2 0.925 0.160 17 39877024 3 prime UTR variant A/C snv 0.40 0.700 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: rs11167764
rs11167764
LOC105378204
2 0.925 0.120 5 142099500 regulatory region variant A/C snv 0.80 0.700 1.000 1 2011 2011
dbSNP: rs1538084
rs1538084 		1 1.000 0.080 1 152523536 intergenic variant A/C snv 0.79 0.700 1.000 1 2011 2011
dbSNP: rs7086533
rs7086533
LINC02660
1 1.000 0.080 10 3926521 intron variant A/C snv 0.91 0.700 1.000 1 2014 2014
dbSNP: rs7219080
rs7219080
GSDMA
1 1.000 0.080 17 39958263 intron variant A/C snv 0.65 0.710 1.000 1 2010 2016
dbSNP: rs1250552
rs1250552
ZMIZ1
5 0.882 0.200 10 79298270 intron variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs13010713
rs13010713
LINC01934
5 0.882 0.200 2 181131318 intron variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs17498196
rs17498196
IL33 ; LOC107987046
2 1.000 0.080 9 6237547 intron variant A/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs241425
rs241425
TAP2
2 0.925 0.160 6 32837132 intron variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs2538026
rs2538026 		1 1.000 0.080 18 56261410 intergenic variant A/C;G snv 0.700 1.000 1 2000 2000
dbSNP: rs9792269
rs9792269 		5 0.882 0.200 8 128252343 intergenic variant A/C;G snv 0.700 1.000 1 2011 2011
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: rs1412426
rs1412426 		1 1.000 0.080 9 6188652 intergenic variant A/C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs10903122
rs10903122 		5 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 0.700 1.000 2 2011 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: rs8067378
rs8067378 		6 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 0.720 1.000 2 2010 2015
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: rs10197862
rs10197862
IL18R1 ; IL1RL1
2 0.925 0.120 2 102350089 intron variant A/G snv 0.18 0.810 1.000 1 2011 2014
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: rs10800812
rs10800812 		1 1.000 0.080 1 202086810 intergenic variant A/G snv 0.77 0.700 1.000 1 2000 2000
dbSNP: rs11747270
rs11747270
IRGM
3 0.790 0.240 5 150879305 intron variant A/G snv 0.21 0.700 1.000 1 2011 2011