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rs13214487

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs13214487(C;G)
Make rs13214487(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354929
GeneHLA-B
is asnp
is mentioned by
dbSNPrs13214487
ebirs13214487
HLIrs13214487
Exacrs13214487
Varsomers13214487
Maprs13214487
PheGenIrs13214487
hapmaprs13214487
1000 genomesrs13214487
hgdprs13214487
ensemblrs13214487
gopubmedrs13214487
geneviewrs13214487
scholarrs13214487
googlers13214487
pharmgkbrs13214487
gwascentralrs13214487
openSNPrs13214487
23andMers13214487
23andMe allrs13214487
SNP Nexus

SNPshotrs13214487
SNPdbers13214487
MSV3drs13214487
GWAS Ctlgrs13214487
GMAF0.03352
Max Magnitude0
ClinVar
Risk rs13214487(G;G)
Alt rs13214487(G;G)
Reference rs13214487(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31322706C>G
CLNSRC
CLNACC