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rs9533156

From SNPedia

Orientationplus
Stabilizedplus
Make rs9533156(C;C)
Make rs9533156(C;T)
Make rs9533156(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position42573535
GeneTNFSF11
is asnp
is mentioned by
dbSNPrs9533156
ebirs9533156
HLIrs9533156
Exacrs9533156
Varsomers9533156
Maprs9533156
PheGenIrs9533156
hapmaprs9533156
1000 genomesrs9533156
hgdprs9533156
ensemblrs9533156
gopubmedrs9533156
geneviewrs9533156
scholarrs9533156
googlers9533156
pharmgkbrs9533156
gwascentralrs9533156
openSNPrs9533156
23andMers9533156
23andMe allrs9533156
SNP Nexus

SNPshotrs9533156
SNPdbers9533156
MSV3drs9533156
GWAS Ctlgrs9533156
GMAF0.4582
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 20231205] Genetic Variations in Genes Encoding RANK, RANKL, and OPG in Rheumatoid Arthritis: A Case-Control Study


[PMID 23369128OA-icon.png] Genetic polymorphism of the OPG gene associated with breast cancer


[PMID 24442994] Association of receptor activator of nuclear factor-kappaB ligand (RANKL) gene polymorphisms with the susceptibility to ankylosing spondylitis: a case-control study


[PMID 23177932] Analysis of RANKL gene polymorphism (rs9533156 and rs2277438) in Iranian patients with chronic periodontitis and periimplantitis.


[PMID 26451891] RANK rs1805034 T>C Polymorphism Is Associated with Susceptibility to Gastric Cardia Adenocarcinoma in a Chinese Population