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rs1055311

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1055311(C;T)
Make rs1055311(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position44289685
GeneAIRE
is asnp
is mentioned by
dbSNPrs1055311
ebirs1055311
HLIrs1055311
Exacrs1055311
Varsomers1055311
Maprs1055311
PheGenIrs1055311
hapmaprs1055311
1000 genomesrs1055311
hgdprs1055311
ensemblrs1055311
gopubmedrs1055311
geneviewrs1055311
scholarrs1055311
googlers1055311
pharmgkbrs1055311
gwascentralrs1055311
openSNPrs1055311
23andMers1055311
23andMe allrs1055311
SNP Nexus

SNPshotrs1055311
SNPdbers1055311
MSV3drs1055311
GWAS Ctlgrs1055311
GMAF0.1368
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 20363194] The role of AIRE polymorphisms in melanoma


ClinVar
Risk rs1055311(T;T)
Alt rs1055311(T;T)
Reference rs1055311(C;C)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene AIRE
CLNDBN not specified
Reversed 0
HGVS NC_000021.8:g.45709568C>T
CLNSRC ClinVar University of Chicago
CLNACC RCV000116302.2,