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rs137854665

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854665(A;A)
Make rs137854665(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356855
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854665
ebirs137854665
HLIrs137854665
Exacrs137854665
Varsomers137854665
Maprs137854665
PheGenIrs137854665
hapmaprs137854665
1000 genomesrs137854665
hgdprs137854665
ensemblrs137854665
gopubmedrs137854665
geneviewrs137854665
scholarrs137854665
googlers137854665
pharmgkbrs137854665
gwascentralrs137854665
openSNPrs137854665
23andMers137854665
23andMe allrs137854665
SNP Nexus

SNPshotrs137854665
SNPdbers137854665
MSV3drs137854665
GWAS Ctlgrs137854665
Max Magnitude0
ClinVar
Risk rs137854665(A,C,T;A,C,T)
Alt rs137854665(A,C,T;A,C,T)
Reference rs137854665(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324632C>A; NC_000006.11:g.31324632C>G; NC_000006.11:g.31324632C>T
CLNSRC
CLNACC