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rs4561508

From SNPedia

Orientationplus
Stabilizedplus
Make rs4561508(C;C)
Make rs4561508(C;T)
Make rs4561508(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position16945436
GeneTNFRSF13B
is asnp
is mentioned by
dbSNPrs4561508
ebirs4561508
HLIrs4561508
Exacrs4561508
Varsomers4561508
Maprs4561508
PheGenIrs4561508
hapmaprs4561508
1000 genomesrs4561508
hgdprs4561508
ensemblrs4561508
gopubmedrs4561508
geneviewrs4561508
scholarrs4561508
googlers4561508
pharmgkbrs4561508
gwascentralrs4561508
openSNPrs4561508
23andMers4561508
23andMe allrs4561508
SNP Nexus

SNPshotrs4561508
SNPdbers4561508
MSV3drs4561508
GWAS Ctlgrs4561508
GMAF0.1827
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23022100OA-icon.png]
Trait Serum total protein level
Title Discovery and fine mapping of serum protein loci through transethnic meta-analysis.
Risk Allele T
P-val 2E-18
Odds Ratio .04 [0.031-0.049] unit increase
GWAS snp
PMID [PMID 23303382]
Trait Hematology traits
Title Genome-wide association study of serum albumin:globulin ratio in Korean populations.
Risk Allele T
P-val 8E-24
Odds Ratio .03 [0.025-0.037] unit increase