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rs4792800

From SNPedia

Orientationplus
Stabilizedplus
Make rs4792800(A;A)
Make rs4792800(A;G)
Make rs4792800(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position16941853
GeneTNFRSF13B
is asnp
is mentioned by
dbSNPrs4792800
ebirs4792800
HLIrs4792800
Exacrs4792800
Varsomers4792800
Maprs4792800
PheGenIrs4792800
hapmaprs4792800
1000 genomesrs4792800
hgdprs4792800
ensemblrs4792800
gopubmedrs4792800
geneviewrs4792800
scholarrs4792800
googlers4792800
pharmgkbrs4792800
gwascentralrs4792800
openSNPrs4792800
23andMers4792800
23andMe allrs4792800
SNP Nexus

SNPshotrs4792800
SNPdbers4792800
MSV3drs4792800
GWAS Ctlgrs4792800
GMAF0.1841
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22673310]
Trait
Title Genome-wide association study identifies common variants at TNFRSF13B associated with IgG level in a healthy Chinese male population.
Risk Allele G
P-val 1E-12
Odds Ratio None None