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rs1419881

From SNPedia

Orientationminus
Stabilizedminus
Make rs1419881(C;C)
Make rs1419881(C;T)
Make rs1419881(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31162816
GeneTCF19
is asnp
is mentioned by
dbSNPrs1419881
ebirs1419881
HLIrs1419881
Exacrs1419881
Varsomers1419881
Maprs1419881
PheGenIrs1419881
hapmaprs1419881
1000 genomesrs1419881
hgdprs1419881
ensemblrs1419881
gopubmedrs1419881
geneviewrs1419881
scholarrs1419881
googlers1419881
pharmgkbrs1419881
gwascentralrs1419881
openSNPrs1419881
23andMers1419881
23andMe allrs1419881
SNP Nexus

SNPshotrs1419881
SNPdbers1419881
MSV3drs1419881
GWAS Ctlgrs1419881
GMAF0.4766
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 1E-18
Odds Ratio 1.37 [1.23-1.52]


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


[PMID 18254969OA-icon.png] Sequence variation in the human transcription factor gene POU5F1.


[PMID 18309376OA-icon.png] Several regions in the major histocompatibility complex confer risk for anti-CCP-antibody positive rheumatoid arthritis, independent of the DRB1 locus.


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


[PMID 27596359] Identification of Novel OCT4 Genetic Variant Associated with the Risk of Chronic Hepatitis B in a Korean Population.


[PMID 27718532] Identification of miRSNPs associated with the risk of multiple myeloma.