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: rs199883290
rs199883290
NOD2
2 0.925 0.120 16 50729867 missense variant G/A;C snv 4.0E-06; 1.5E-02 7.0E-06 0.700 1.000 4 2007 2012
dbSNP: rs540973741
rs540973741
NOD2
2 0.925 0.120 16 50729868 frameshift variant C/-;CC delins 0.700 1.000 4 2007 2012
dbSNP: rs2858331
rs2858331 		5 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 0.700 1.000 2 2008 2013
dbSNP: rs1002922
rs1002922 		1 1.000 0.040 5 40386453 regulatory region variant T/C snv 0.29 0.700 1.000 1 2007 2007
dbSNP: rs10117785
rs10117785
TNFSF15
1 1.000 0.040 9 114789323 3 prime UTR variant T/A snv 0.34 0.700 1.000 1 2005 2005
dbSNP: rs10484545
rs10484545
LOC101929006
1 1.000 0.040 6 29266733 intron variant C/A;G snv 0.700 1.000 1 2007 2007
dbSNP: rs10489276
rs10489276 		1 1.000 0.040 1 172893799 intron variant C/T snv 0.31 0.700 1.000 1 2008 2008
dbSNP: rs10489629
rs10489629
IL23R ; C1orf141
1 0.827 0.240 1 67222666 intron variant T/C snv 0.48 0.700 1.000 1 2006 2006
dbSNP: rs10512734
rs10512734 		1 1.000 0.040 5 40393503 intergenic variant A/C;G snv 0.29 0.700 1.000 1 2007 2007
dbSNP: rs1063355
rs1063355
HLA-DQB1 ; HLA-DQB1-AS1
2 0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs10886462
rs10886462
GRK5
1 1.000 0.040 10 119345799 intron variant A/G snv 0.22 0.700 1.000 1 2007 2007
dbSNP: rs1105267
rs1105267 		1 1.000 0.040 13 20365097 intergenic variant G/A snv 0.54 0.700 1.000 1 2006 2006
dbSNP: rs1109863
rs1109863 		1 1.000 0.040 16 50658453 intergenic variant G/A snv 0.69 0.700 1.000 1 2007 2007
dbSNP: rs11208994
rs11208994 		1 1.000 0.040 1 67059360 regulatory region variant A/G;T snv 0.700 1.000 1 2007 2007
dbSNP: rs11209008
rs11209008
IL23R ; C1orf141
1 0.882 0.080 1 67157615 intron variant G/A;T snv 5.7E-02 0.700 1.000 1 2007 2007
dbSNP: rs11265519
rs11265519 		1 1.000 0.040 1 160909123 intergenic variant C/A snv 0.60 0.700 1.000 1 2008 2008
dbSNP: rs1142287
rs1142287
SCAMP3
1 1.000 0.040 1 155260340 synonymous variant C/T snv 0.34 0.36 0.700 1.000 1 2010 2010
dbSNP: rs11640716
rs11640716
NKD1
1 1.000 0.040 16 50631178 intron variant T/A;G snv 0.700 1.000 1 2007 2007
dbSNP: rs11718165
rs11718165
BSN
1 1.000 0.040 3 49659364 intron variant A/G snv 0.27 0.700 1.000 1 2007 2007
dbSNP: rs11804284
rs11804284
IL23R
1 1.000 0.040 1 67233571 intron variant T/A;C;G snv 0.700 1.000 1 2007 2007
dbSNP: rs12521097
rs12521097
P4HA2
1 1.000 0.040 5 132239645 intron variant G/A snv 0.42 0.700 1.000 1 2007 2007
dbSNP: rs12529198
rs12529198
LYRM4 ; LYRM4-AS1
1 1.000 0.040 6 5151013 intron variant A/G snv 9.9E-02 0.700 1.000 1 2008 2008
dbSNP: rs12552933
rs12552933 		1 1.000 0.040 9 114759302 intergenic variant C/T snv 2.9E-02 0.700 1.000 1 2013 2013
dbSNP: rs12576495
rs12576495 		1 1.000 0.040 11 93131841 upstream gene variant T/C snv 0.23 0.700 1.000 1 2007 2007
dbSNP: rs12913
rs12913
NKD1
1 1.000 0.040 16 50634515 3 prime UTR variant T/C snv 0.61 0.700 1.000 1 2007 2007