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rs17695092

From SNPedia

Orientationplus
Stabilizedplus
Make rs17695092(G;G)
Make rs17695092(G;T)
Make rs17695092(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position173910850
GeneCPEB4
is asnp
is mentioned by
dbSNPrs17695092
dbSNP (classic)rs17695092
ClinGenrs17695092
ebirs17695092
HLIrs17695092
Exacrs17695092
Gnomadrs17695092
Varsomers17695092
LitVarrs17695092
Maprs17695092
PheGenIrs17695092
Biobankrs17695092
1000 genomesrs17695092
hgdprs17695092
ensemblrs17695092
geneviewrs17695092
scholarrs17695092
googlers17695092
pharmgkbrs17695092
gwascentralrs17695092
openSNPrs17695092
23andMers17695092
SNPshotrs17695092
SNPdbers17695092
MSV3drs17695092
GWAS Ctlgrs17695092
GMAF0.1635
Max Magnitude0
? (G;G) (G;T) (T;T) 28


GWAS snp
PMID [PMID 23128233OA-icon.png]
Trait Crohn's disease
Title Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Risk Allele T
P-val 5E-9
Odds Ratio 1.10 [1.055-1.136]