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rs4985726

From SNPedia

Orientationplus
Stabilizedplus
Make rs4985726(C;C)
Make rs4985726(C;G)
Make rs4985726(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position16960324
GeneTNFRSF13B
is asnp
is mentioned by
dbSNPrs4985726
ebirs4985726
HLIrs4985726
Exacrs4985726
Varsomers4985726
Maprs4985726
PheGenIrs4985726
hapmaprs4985726
1000 genomesrs4985726
hgdprs4985726
ensemblrs4985726
gopubmedrs4985726
geneviewrs4985726
scholarrs4985726
googlers4985726
pharmgkbrs4985726
gwascentralrs4985726
openSNPrs4985726
23andMers4985726
23andMe allrs4985726
SNP Nexus

SNPshotrs4985726
SNPdbers4985726
MSV3drs4985726
GWAS Ctlgrs4985726
GMAF0.1694
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 22558069OA-icon.png]
Trait
Title Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese.
Risk Allele G
P-val 7E-24
Odds Ratio 0.1350 None