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: rs13314993
rs13314993
LOC105377022
5 0.882 0.200 3 32973977 regulatory region variant G/C;T snv 0.700 1.000 2 2011 2011
dbSNP: rs13408661
rs13408661
IL18R1 ; IL1RL1
2 1.000 0.080 2 102338622 intron variant G/A snv 0.18 0.810 1.000 2 2011 2012
dbSNP: rs1464510
rs1464510
LPP
7 0.807 0.280 3 188394766 intron variant C/A;T snv 0.700 1.000 2 2011 2011
dbSNP: rs1736135
rs1736135
LOC101927745
4 0.851 0.160 21 15432901 intron variant T/C snv 0.33 0.700 1.000 2 2011 2011
dbSNP: rs4794820
rs4794820
LRRC3C
3 0.790 0.160 17 39933091 intron variant A/G;T snv 0.810 1.000 2 2011 2012
dbSNP: rs6503525
rs6503525
LRRC3C
2 0.925 0.080 17 39938921 intron variant G/A;C snv 0.810 1.000 2 2011 2015
dbSNP: rs802734
rs802734 		5 0.827 0.280 6 127957653 intergenic variant A/G;T snv 0.700 1.000 2 2011 2011
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: rs1008723
rs1008723
GSDMB
3 0.925 0.160 17 39910014 intron variant G/C;T snv 0.800 1.000 1 2011 2019
dbSNP: rs10173081
rs10173081
IL18R1 ; IL1RL1
2 1.000 0.080 2 102340888 intron variant C/T snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs10189629
rs10189629 		2 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 0.700 1.000 1 2011 2011
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: rs1043828
rs1043828
WDR36
2 1.000 0.080 5 111128310 3 prime UTR variant T/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs10445308
rs10445308
IKZF3
3 0.851 0.240 17 39781794 intron variant C/T snv 0.38 0.700 1.000 1 2011 2011
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: 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: 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: rs10758669
rs10758669 		5 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10806425
rs10806425
BACH2
5 0.851 0.280 6 90216893 intron variant C/A snv 0.33 0.700 1.000 1 2011 2011
dbSNP: rs10995271
rs10995271 		3 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 0.700 1.000 1 2011 2011
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: rs11078925
rs11078925
ZPBP2
3 0.925 0.160 17 39868955 intron variant T/C snv 0.36 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