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rs878081

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878081(C;T)
Make rs878081(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome21
Position44288394
GeneAIRE
is asnp
is mentioned by
dbSNPrs878081
ebirs878081
HLIrs878081
Exacrs878081
Varsomers878081
Maprs878081
PheGenIrs878081
hapmaprs878081
1000 genomesrs878081
hgdprs878081
ensemblrs878081
gopubmedrs878081
geneviewrs878081
scholarrs878081
googlers878081
pharmgkbrs878081
gwascentralrs878081
openSNPrs878081
23andMers878081
23andMe allrs878081
SNP Nexus

SNPshotrs878081
SNPdbers878081
MSV3drs878081
GWAS Ctlgrs878081
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs878081(T;T)
Alt rs878081(T;T)
Reference rs878081(C;C)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene AIRE
CLNDBN not specified
Reversed 0
HGVS NC_000021.8:g.45708277C>T
CLNSRC
CLNACC RCV000116301.2,



[PMID 27264825] [Association of AIRE gene polymorphisms with susceptibility to rheumatoid arthritis among ethnic Han Chinese from Shaanxi].