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rs3132687

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3132687(C;T)
Make rs3132687(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943579
GeneHLA-A
is asnp
is mentioned by
dbSNPrs3132687
ebirs3132687
HLIrs3132687
Exacrs3132687
Varsomers3132687
Maprs3132687
PheGenIrs3132687
hapmaprs3132687
1000 genomesrs3132687
hgdprs3132687
ensemblrs3132687
gopubmedrs3132687
geneviewrs3132687
scholarrs3132687
googlers3132687
pharmgkbrs3132687
gwascentralrs3132687
openSNPrs3132687
23andMers3132687
23andMe allrs3132687
SNP Nexus

SNPshotrs3132687
SNPdbers3132687
MSV3drs3132687
GWAS Ctlgrs3132687
GMAF0.1556
Max Magnitude0
ClinVar
Risk rs3132687(T;T)
Alt rs3132687(T;T)
Reference rs3132687(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 1
HGVS NC_000006.11:g.29911356G; NC_000006.11:g.29911356G>A
CLNSRC
CLNACC