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rs2856718

From SNPedia

Orientationminus
Stabilizedminus
Make rs2856718(A;A)
Make rs2856718(A;G)
Make rs2856718(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32702478
is asnp
is mentioned by
dbSNPrs2856718
ebirs2856718
HLIrs2856718
Exacrs2856718
Varsomers2856718
Maprs2856718
PheGenIrs2856718
hapmaprs2856718
1000 genomesrs2856718
hgdprs2856718
ensemblrs2856718
gopubmedrs2856718
geneviewrs2856718
scholarrs2856718
googlers2856718
pharmgkbrs2856718
gwascentralrs2856718
openSNPrs2856718
23andMers2856718
23andMe allrs2856718
SNP Nexus

SNPshotrs2856718
SNPdbers2856718
MSV3drs2856718
GWAS Ctlgrs2856718
GMAF0.3848
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 21750111] A Genome-Wide Association Study of Chronic Hepatitis B Identified Novel Risk Locus in a Japanese Population


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


[PMID 19707526OA-icon.png] European population genetic substructure: further definition of ancestry informative markers for distinguishing among diverse European ethnic groups.


[PMID 20018067OA-icon.png] A two-stage search strategy for detecting multiple loci associated with rheumatoid arthritis.


[PMID 22105689] Genetic variants in human leukocyte antigen/DP-DQ influence both hepatitis B virus clearance and hepatocellular carcinoma development.

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 2E-24
Odds Ratio 1.60 [1.46-1.75]


[PMID 23428460] Genetic variants in HLA-DP/DQ contribute to risk of cervical cancer: a two-stage study in Chinese women.


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


[PMID 25376093OA-icon.png] Association between single-nucleotide polymorphisms and early spontaneous hepatitis B virus e antigen seroconversion in children