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rs77882874

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs77882874(C;T)
Make rs77882874(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356952
GeneHLA-B
is asnp
is mentioned by
dbSNPrs77882874
ebirs77882874
HLIrs77882874
Exacrs77882874
Varsomers77882874
Maprs77882874
PheGenIrs77882874
hapmaprs77882874
1000 genomesrs77882874
hgdprs77882874
ensemblrs77882874
gopubmedrs77882874
geneviewrs77882874
scholarrs77882874
googlers77882874
pharmgkbrs77882874
gwascentralrs77882874
openSNPrs77882874
23andMers77882874
23andMe allrs77882874
SNP Nexus

SNPshotrs77882874
SNPdbers77882874
MSV3drs77882874
GWAS Ctlgrs77882874
Max Magnitude0
ClinVar
Risk rs77882874(T;T)
Alt rs77882874(T;T)
Reference rs77882874(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324729G>A
CLNSRC
CLNACC