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rs652888

From SNPedia

Orientationminus
Stabilizedminus
Make rs652888(C;C)
Make rs652888(C;T)
Make rs652888(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31883457
GeneEHMT2
is asnp
is mentioned by
dbSNPrs652888
ebirs652888
HLIrs652888
Exacrs652888
Varsomers652888
Maprs652888
PheGenIrs652888
hapmaprs652888
1000 genomesrs652888
hgdprs652888
ensemblrs652888
gopubmedrs652888
geneviewrs652888
scholarrs652888
googlers652888
pharmgkbrs652888
gwascentralrs652888
openSNPrs652888
23andMers652888
23andMe allrs652888
SNP Nexus

SNPshotrs652888
SNPdbers652888
MSV3drs652888
GWAS Ctlgrs652888
GMAF0.1983
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23760081]
Trait Chronic hepatitis B infection
Title A genome-wide association study identified new variants associated with the risk of chronic hepatitis B.
Risk Allele
P-val 7E-13
Odds Ratio 1.38 [1.22-1.57]


[PMID 24465836OA-icon.png] Genetic association of human leukocyte antigens with chronicity or resolution of hepatitis B infection in thai population


[PMID 18204098] Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.


[PMID 25802187] Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B


[PMID 27157822] Genetic variants associated with antithyroid drug-induced agranulocytosis: a genome-wide association study in a European population.