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rs45560938

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs45560938(G;G)
Make rs45560938(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357084
GeneHLA-B
is asnp
is mentioned by
dbSNPrs45560938
ebirs45560938
HLIrs45560938
Exacrs45560938
Varsomers45560938
Maprs45560938
PheGenIrs45560938
hapmaprs45560938
1000 genomesrs45560938
hgdprs45560938
ensemblrs45560938
gopubmedrs45560938
geneviewrs45560938
scholarrs45560938
googlers45560938
pharmgkbrs45560938
gwascentralrs45560938
openSNPrs45560938
23andMers45560938
23andMe allrs45560938
SNP Nexus

SNPshotrs45560938
SNPdbers45560938
MSV3drs45560938
GWAS Ctlgrs45560938
Max Magnitude0
ClinVar
Risk rs45560938(G;G)
Alt rs45560938(G;G)
Reference rs45560938(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324861A>C
CLNSRC
CLNACC