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rs9264638

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9264638(A;A)
Make rs9264638(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270541
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264638
dbSNP (classic)rs9264638
ClinGenrs9264638
ebirs9264638
HLIrs9264638
Exacrs9264638
Gnomadrs9264638
Varsomers9264638
LitVarrs9264638
Maprs9264638
PheGenIrs9264638
Biobankrs9264638
1000 genomesrs9264638
hgdprs9264638
ensemblrs9264638
geneviewrs9264638
scholarrs9264638
googlers9264638
pharmgkbrs9264638
gwascentralrs9264638
openSNPrs9264638
23andMers9264638
SNPshotrs9264638
SNPdbers9264638
MSV3drs9264638
GWAS Ctlgrs9264638
GMAF0.253
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23417110OA-icon.png]
Trait Beta-2 microglubulin plasma levels
Title Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.
Risk Allele A
P-val 2E-23
Odds Ratio .04 [0.032-0.048] unit decrease
ClinVar
Risk rs9264638(A;A)
Alt rs9264638(A;A)
Reference Rs9264638(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31238318G>A
CLNSRC
CLNACC