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rs137854638

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137854638(A;G)
Make rs137854638(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356946
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854638
ebirs137854638
HLIrs137854638
Exacrs137854638
Varsomers137854638
Maprs137854638
PheGenIrs137854638
hapmaprs137854638
1000 genomesrs137854638
hgdprs137854638
ensemblrs137854638
gopubmedrs137854638
geneviewrs137854638
scholarrs137854638
googlers137854638
pharmgkbrs137854638
gwascentralrs137854638
openSNPrs137854638
23andMers137854638
23andMe allrs137854638
SNP Nexus

SNPshotrs137854638
SNPdbers137854638
MSV3drs137854638
GWAS Ctlgrs137854638
Max Magnitude0
ClinVar
Risk rs137854638(G,T;G,T)
Alt rs137854638(G,T;G,T)
Reference rs137854638(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324723T>A; NC_000006.11:g.31324723T>C
CLNSRC
CLNACC