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: rs2076756
rs2076756
NOD2
2 0.882 0.040 16 50722970 intron variant A/G snv 0.17 0.830 1.000 6 2007 2019
dbSNP: rs9858542
rs9858542
BSN
2 0.925 0.040 3 49664550 synonymous variant G/A snv 0.26 0.27 0.810 1.000 3 2007 2010
dbSNP: rs11742570
rs11742570 		2 0.925 0.040 5 40410482 upstream gene variant T/C;G snv 0.800 1.000 2 2010 2017
dbSNP: rs17221417
rs17221417
NOD2
1 0.925 0.040 16 50705671 intron variant C/G snv 0.20 0.810 1.000 2 2007 2017
dbSNP: rs17309827
rs17309827
SLC22A23
1 1.000 0.040 6 3433084 intron variant T/G snv 0.30 0.800 1.000 2 2008 2010
dbSNP: rs1736020
rs1736020
LOC101927745
1 1.000 0.040 21 15440233 intron variant C/A snv 0.33 0.800 1.000 2 2008 2010
dbSNP: rs3792109
rs3792109
ATG16L1 ; SCARNA5
1 1.000 0.040 2 233275771 non coding transcript exon variant G/A snv 0.45 0.42 0.800 1.000 2 2010 2013
dbSNP: rs5743289
rs5743289
NOD2
2 1.000 0.040 16 50722863 intron variant C/G;T snv 0.810 1.000 2 2007 2014
dbSNP: rs7702331
rs7702331
LOC105379031
1 1.000 0.040 5 73255307 intron variant A/G snv 0.42 0.800 1.000 2 2010 2012
dbSNP: rs1000113
rs1000113
IRGM
1 0.925 0.040 5 150860514 intron variant C/T snv 0.13 0.840 1.000 1 2007 2015
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: rs10065637
rs10065637
ANKRD55
1 1.000 0.040 5 56143024 intron variant C/T snv 0.15 0.800 1.000 1 2012 2012
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: rs10181042
rs10181042
PUS10
1 1.000 0.040 2 60997124 intron variant C/T snv 0.41 0.800 1.000 1 2010 2010
dbSNP: rs10210302
rs10210302
ATG16L1
1 1.000 0.040 2 233250193 intron variant C/A;T snv 0.810 1.000 1 2007 2010
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: rs10486483
rs10486483
SKAP2
1 1.000 0.040 7 26852821 intron variant G/A snv 0.21 0.800 1.000 1 2012 2015
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: rs10495903
rs10495903
THADA
2 1.000 0.040 2 43579779 intron variant C/T snv 0.13 0.800 1.000 1 2010 2017
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: rs10734105
rs10734105 		1 1.000 0.040 10 131373856 intergenic variant G/A;C;T snv 0.800 1.000 1 2012 2012
dbSNP: rs10761659
rs10761659 		2 0.925 0.040 10 62685804 intron variant A/G snv 0.43 0.810 1.000 1 2010 2017
dbSNP: rs10789230
rs10789230 		1 1.000 0.040 1 67264945 downstream gene variant G/C;T snv 0.800 1.000 1 2007 2007
dbSNP: rs10801047
rs10801047 		1 1.000 0.040 1 191590226 intergenic variant A/T snv 0.82 0.800 1.000 1 2007 2007
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