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rs137854659

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137854659(C;C)
Make rs137854659(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356880
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854659
ebirs137854659
HLIrs137854659
Exacrs137854659
Varsomers137854659
Maprs137854659
PheGenIrs137854659
hapmaprs137854659
1000 genomesrs137854659
hgdprs137854659
ensemblrs137854659
gopubmedrs137854659
geneviewrs137854659
scholarrs137854659
googlers137854659
pharmgkbrs137854659
gwascentralrs137854659
openSNPrs137854659
23andMers137854659
23andMe allrs137854659
SNP Nexus

SNPshotrs137854659
SNPdbers137854659
MSV3drs137854659
GWAS Ctlgrs137854659
Max Magnitude0
ClinVar
Risk rs137854659(A,C;A,C)
Alt rs137854659(A,C;A,C)
Reference rs137854659(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324657A>G; NC_000006.11:g.31324657A>T
CLNSRC
CLNACC