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rs76827460

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs76827460(A;G)
Make rs76827460(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356868
GeneHLA-B
is asnp
is mentioned by
dbSNPrs76827460
ClinGenrs76827460
ebirs76827460
HLIrs76827460
Exacrs76827460
Varsomers76827460
Maprs76827460
PheGenIrs76827460
hapmaprs76827460
1000 genomesrs76827460
hgdprs76827460
ensemblrs76827460
gopubmedrs76827460
geneviewrs76827460
scholarrs76827460
googlers76827460
pharmgkbrs76827460
gwascentralrs76827460
openSNPrs76827460
23andMers76827460
23andMe allrs76827460
SNP Nexus

SNPshotrs76827460
SNPdbers76827460
MSV3drs76827460
GWAS Ctlgrs76827460
Max Magnitude0
ClinVar
Risk rs76827460(G;G)
Alt rs76827460(G;G)
Reference Rs76827460(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324645T>C
CLNSRC
CLNACC