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rs137854673

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854673(A;A)
Make rs137854673(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356836
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854673
ebirs137854673
HLIrs137854673
Exacrs137854673
Varsomers137854673
Maprs137854673
PheGenIrs137854673
hapmaprs137854673
1000 genomesrs137854673
hgdprs137854673
ensemblrs137854673
gopubmedrs137854673
geneviewrs137854673
scholarrs137854673
googlers137854673
pharmgkbrs137854673
gwascentralrs137854673
openSNPrs137854673
23andMers137854673
23andMe allrs137854673
SNP Nexus

SNPshotrs137854673
SNPdbers137854673
MSV3drs137854673
GWAS Ctlgrs137854673
Max Magnitude0
ClinVar
Risk rs137854673(A,T;A,T)
Alt rs137854673(A,T;A,T)
Reference rs137854673(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324613C>A; NC_000006.11:g.31324613C>T
CLNSRC
CLNACC