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rs12663356

From SNPedia

Orientationplus
Stabilizedplus
Make rs12663356(C;C)
Make rs12663356(C;T)
Make rs12663356(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position21430497
is asnp
is mentioned by
dbSNPrs12663356
dbSNP (classic)rs12663356
ClinGenrs12663356
ebirs12663356
HLIrs12663356
Exacrs12663356
Gnomadrs12663356
Varsomers12663356
LitVarrs12663356
Maprs12663356
PheGenIrs12663356
Biobankrs12663356
1000 genomesrs12663356
hgdprs12663356
ensemblrs12663356
geneviewrs12663356
scholarrs12663356
googlers12663356
pharmgkbrs12663356
gwascentralrs12663356
openSNPrs12663356
23andMers12663356
SNPshotrs12663356
SNPdbers12663356
MSV3drs12663356
GWAS Ctlgrs12663356
GMAF0.4844
Max Magnitude0
? (C;C) (C;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 C
P-val 4E-12
Odds Ratio 1.10 [1.06-1.131]