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rs4639334

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 1.5 Homozygous for HLA-DQ7 haplotype
(A;G) 1.5 Single HLA-DQ7 haplotype
Make rs4639334(G;G)
ReferenceGRCh37 37.1/131
Chromosome6
Position32634437
GeneLOC107987449, LOC107987459
is asnp
is mentioned by
dbSNPrs4639334
dbSNP (classic)rs4639334
ClinGenrs4639334
ebirs4639334
HLIrs4639334
Exacrs4639334
Gnomadrs4639334
Varsomers4639334
LitVarrs4639334
Maprs4639334
PheGenIrs4639334
Biobankrs4639334
1000 genomesrs4639334
hgdprs4639334
ensemblrs4639334
geneviewrs4639334
scholarrs4639334
googlers4639334
pharmgkbrs4639334
gwascentralrs4639334
openSNPrs4639334
23andMers4639334
SNPshotrs4639334
SNPdbers4639334
MSV3drs4639334
GWAS Ctlgrs4639334
Max Magnitude1.5
? (A;A) (A;G) (G;G) 28


rs4639334(A) is said to tag (i.e. identify the presence of) the HLA-DQ7 haplotype, at least in UK populations.[PMID 18509540OA-icon.png]

Source nature

Graves' disease or myasthenia gravis rs3129763(C) + rs4639334(C)


[PMID 19846760OA-icon.png] Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases.