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rs6837335

From SNPedia

Orientationplus
Stabilizedplus
Make rs6837335(A;A)
Make rs6837335(A;G)
Make rs6837335(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position48361966
GeneSLAIN2
is asnp
is mentioned by
dbSNPrs6837335
ebirs6837335
HLIrs6837335
Exacrs6837335
Varsomers6837335
Maprs6837335
PheGenIrs6837335
hapmaprs6837335
1000 genomesrs6837335
hgdprs6837335
ensemblrs6837335
gopubmedrs6837335
geneviewrs6837335
scholarrs6837335
googlers6837335
pharmgkbrs6837335
gwascentralrs6837335
openSNPrs6837335
23andMers6837335
23andMe allrs6837335
SNP Nexus

SNPshotrs6837335
SNPdbers6837335
MSV3drs6837335
GWAS Ctlgrs6837335
GMAF0.4624
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 2E-8
Odds Ratio 1.09 [1.049-1.123]