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rs4819388

From SNPedia

Orientationplus
Stabilizedplus
Make rs4819388(C;C)
Make rs4819388(C;T)
Make rs4819388(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position44227538
GeneICOSLG
is asnp
is mentioned by
dbSNPrs4819388
ebirs4819388
HLIrs4819388
Exacrs4819388
Varsomers4819388
Maprs4819388
PheGenIrs4819388
hapmaprs4819388
1000 genomesrs4819388
hgdprs4819388
ensemblrs4819388
gopubmedrs4819388
geneviewrs4819388
scholarrs4819388
googlers4819388
pharmgkbrs4819388
gwascentralrs4819388
openSNPrs4819388
23andMers4819388
23andMe allrs4819388
SNP Nexus

SNPshotrs4819388
SNPdbers4819388
MSV3drs4819388
GWAS Ctlgrs4819388
GMAF0.287
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20190752OA-icon.png]
Trait Celiac disease
Title Multiple common variants for celiac disease influencing immune gene expression
Risk Allele
P-val 2E-9
Odds Ratio 1.14 [1.09-1.19]


[PMID 23688438] A functional variant at miR-24 binding site in B7-H2 alters susceptibility to gastric cancer in a Chinese Han population


[PMID 22592522] Association of celiac disease genes with inflammatory bowel disease in Finnish and Swedish patients.


[PMID 23543094OA-icon.png] Testing for associations between loci and environmental gradients using latent factor mixed models.