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rs79650563

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs79650563(A;A)
Make rs79650563(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356228
GeneHLA-B
is asnp
is mentioned by
dbSNPrs79650563
ebirs79650563
HLIrs79650563
Exacrs79650563
Varsomers79650563
Maprs79650563
PheGenIrs79650563
hapmaprs79650563
1000 genomesrs79650563
hgdprs79650563
ensemblrs79650563
gopubmedrs79650563
geneviewrs79650563
scholarrs79650563
googlers79650563
pharmgkbrs79650563
gwascentralrs79650563
openSNPrs79650563
23andMers79650563
23andMe allrs79650563
SNP Nexus

SNPshotrs79650563
SNPdbers79650563
MSV3drs79650563
GWAS Ctlgrs79650563
Max Magnitude0
ClinVar
Risk rs79650563(A,T;A,T)
Alt rs79650563(A,T;A,T)
Reference rs79650563(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324005G>A; NC_000006.11:g.31324005G>T
CLNSRC
CLNACC