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rs137854768

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854768(A;A)
Make rs137854768(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356221
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854768
ebirs137854768
HLIrs137854768
Exacrs137854768
Varsomers137854768
Maprs137854768
PheGenIrs137854768
hapmaprs137854768
1000 genomesrs137854768
hgdprs137854768
ensemblrs137854768
gopubmedrs137854768
geneviewrs137854768
scholarrs137854768
googlers137854768
pharmgkbrs137854768
gwascentralrs137854768
openSNPrs137854768
23andMers137854768
23andMe allrs137854768
SNP Nexus

SNPshotrs137854768
SNPdbers137854768
MSV3drs137854768
GWAS Ctlgrs137854768
Max Magnitude0
ClinVar
Risk rs137854768(A,C;A,C)
Alt rs137854768(A,C;A,C)
Reference rs137854768(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323998C>G; NC_000006.11:g.31323998C>T
CLNSRC
CLNACC