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rs4837656

From SNPedia

Orientationplus
Stabilizedplus
Make rs4837656(C;C)
Make rs4837656(C;T)
Make rs4837656(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position119671775
is asnp
is mentioned by
dbSNPrs4837656
ebirs4837656
HLIrs4837656
Exacrs4837656
Varsomers4837656
Maprs4837656
PheGenIrs4837656
hapmaprs4837656
1000 genomesrs4837656
hgdprs4837656
ensemblrs4837656
gopubmedrs4837656
geneviewrs4837656
scholarrs4837656
googlers4837656
pharmgkbrs4837656
gwascentralrs4837656
openSNPrs4837656
23andMers4837656
23andMe allrs4837656
SNP Nexus

SNPshotrs4837656
SNPdbers4837656
MSV3drs4837656
GWAS Ctlgrs4837656
GMAF0.2112
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 22703024] Toll-like receptor gene polymorphisms confer susceptibility to graft-versus-host disease in allogenic hematopoietic stem cell transplantation