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rs137854651

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854651(C;G)
Make rs137854651(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356910
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854651
ebirs137854651
HLIrs137854651
Exacrs137854651
Varsomers137854651
Maprs137854651
PheGenIrs137854651
hapmaprs137854651
1000 genomesrs137854651
hgdprs137854651
ensemblrs137854651
gopubmedrs137854651
geneviewrs137854651
scholarrs137854651
googlers137854651
pharmgkbrs137854651
gwascentralrs137854651
openSNPrs137854651
23andMers137854651
23andMe allrs137854651
SNP Nexus

SNPshotrs137854651
SNPdbers137854651
MSV3drs137854651
GWAS Ctlgrs137854651
Max Magnitude0
ClinVar
Risk rs137854651(G,T;G,T)
Alt rs137854651(G,T;G,T)
Reference rs137854651(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324687G>A; NC_000006.11:g.31324687G>C
CLNSRC
CLNACC