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rs4552569

From SNPedia

Orientationplus
Stabilizedplus
Make rs4552569(C;C)
Make rs4552569(C;T)
Make rs4552569(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position83877774
is asnp
is mentioned by
dbSNPrs4552569
dbSNP (classic)rs4552569
ClinGenrs4552569
ebirs4552569
HLIrs4552569
Exacrs4552569
Gnomadrs4552569
Varsomers4552569
LitVarrs4552569
Maprs4552569
PheGenIrs4552569
Biobankrs4552569
1000 genomesrs4552569
hgdprs4552569
ensemblrs4552569
geneviewrs4552569
scholarrs4552569
googlers4552569
pharmgkbrs4552569
gwascentralrs4552569
openSNPrs4552569
23andMers4552569
SNPshotrs4552569
SNPdbers4552569
MSV3drs4552569
GWAS Ctlgrs4552569
GMAF0.2672
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 22138694] A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis


[PMID 30262694] Association of rs4552569 and rs17095830 single-nucleotide polymorphisms with susceptibility to ankylosing spondylitis in east Asian population: a meta-analysis.