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rs45532737

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45532737(C;G)
Make rs45532737(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356384
GeneHLA-B
is asnp
is mentioned by
dbSNPrs45532737
ebirs45532737
HLIrs45532737
Exacrs45532737
Varsomers45532737
Maprs45532737
PheGenIrs45532737
hapmaprs45532737
1000 genomesrs45532737
hgdprs45532737
ensemblrs45532737
gopubmedrs45532737
geneviewrs45532737
scholarrs45532737
googlers45532737
pharmgkbrs45532737
gwascentralrs45532737
openSNPrs45532737
23andMers45532737
23andMe allrs45532737
SNP Nexus

SNPshotrs45532737
SNPdbers45532737
MSV3drs45532737
GWAS Ctlgrs45532737
Max Magnitude0
ClinVar
Risk rs45532737(G,T;G,T)
Alt rs45532737(G,T;G,T)
Reference rs45532737(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324161G>A; NC_000006.11:g.31324161G>C
CLNSRC
CLNACC