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rs79051037

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs79051037(A;A)
Make rs79051037(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356918
GeneHLA-B
is asnp
is mentioned by
dbSNPrs79051037
ebirs79051037
HLIrs79051037
Exacrs79051037
Varsomers79051037
Maprs79051037
PheGenIrs79051037
hapmaprs79051037
1000 genomesrs79051037
hgdprs79051037
ensemblrs79051037
gopubmedrs79051037
geneviewrs79051037
scholarrs79051037
googlers79051037
pharmgkbrs79051037
gwascentralrs79051037
openSNPrs79051037
23andMers79051037
23andMe allrs79051037
SNP Nexus

SNPshotrs79051037
SNPdbers79051037
MSV3drs79051037
GWAS Ctlgrs79051037
Max Magnitude0
ClinVar
Risk rs79051037(A;A)
Alt rs79051037(A;A)
Reference rs79051037(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324695C>T
CLNSRC
CLNACC