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rs1133779

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1133779(C;C)
Make rs1133779(C;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position44297667
GeneAIRE
is asnp
is mentioned by
dbSNPrs1133779
ebirs1133779
HLIrs1133779
Exacrs1133779
Varsomers1133779
Maprs1133779
PheGenIrs1133779
hapmaprs1133779
1000 genomesrs1133779
hgdprs1133779
ensemblrs1133779
gopubmedrs1133779
geneviewrs1133779
scholarrs1133779
googlers1133779
pharmgkbrs1133779
gwascentralrs1133779
openSNPrs1133779
23andMers1133779
23andMe allrs1133779
SNP Nexus

SNPshotrs1133779
SNPdbers1133779
MSV3drs1133779
GWAS Ctlgrs1133779
Merged fromRs1800522
GMAF0.4573
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 20363194] The role of AIRE polymorphisms in melanoma.

ClinVar
Risk rs1133779(C;C)
Alt rs1133779(C;C)
Reference rs1133779(T;T)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene AIRE
CLNDBN not specified
Reversed 0
HGVS NC_000021.8:g.45717550T>C
CLNSRC ClinVar University of Chicago
CLNACC RCV000116300.2,