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rs4809330

From SNPedia

Orientationplus
Stabilizedplus
Make rs4809330(A;A)
Make rs4809330(A;G)
Make rs4809330(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position63718234
GeneZGPAT
is asnp
is mentioned by
dbSNPrs4809330
ebirs4809330
HLIrs4809330
Exacrs4809330
Varsomers4809330
Maprs4809330
PheGenIrs4809330
hapmaprs4809330
1000 genomesrs4809330
hgdprs4809330
ensemblrs4809330
gopubmedrs4809330
geneviewrs4809330
scholarrs4809330
googlers4809330
pharmgkbrs4809330
gwascentralrs4809330
openSNPrs4809330
23andMers4809330
23andMe allrs4809330
SNP Nexus

SNPshotrs4809330
SNPdbers4809330
MSV3drs4809330
GWAS Ctlgrs4809330
GMAF0.3251
Max Magnitude
? (A;A) (A;G) (G;G) 28
OMIM612566
DescINFLAMMATORY BOWEL DISEASE 24; IBD24
Variant
Relatedalso


[PMID 20187130] Evidence of epistasis between TNFRSF14 and TNFRSF6B polymorphisms in patients with rheumatoid arthritis

GWAS snp
PMID [PMID 21102463OA-icon.png]
Trait
Title Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Risk Allele G
P-val 3E-15
Odds Ratio 1.1200 [1.06-1.18]


[PMID 20962851] Members 6B and 14 of the TNF receptor superfamily in multiple sclerosis predisposition


[PMID 18758464OA-icon.png] Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease.


[PMID 19623168] Investigation of reported associations between the 20q13 and 21q22 loci and pediatric-onset Crohn's disease in Canadian children.