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rs137854656

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854656(C;G)
Make rs137854656(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356893
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854656
ebirs137854656
HLIrs137854656
Exacrs137854656
Varsomers137854656
Maprs137854656
PheGenIrs137854656
hapmaprs137854656
1000 genomesrs137854656
hgdprs137854656
ensemblrs137854656
gopubmedrs137854656
geneviewrs137854656
scholarrs137854656
googlers137854656
pharmgkbrs137854656
gwascentralrs137854656
openSNPrs137854656
23andMers137854656
23andMe allrs137854656
SNP Nexus

SNPshotrs137854656
SNPdbers137854656
MSV3drs137854656
GWAS Ctlgrs137854656
Max Magnitude0
ClinVar
Risk rs137854656(G,T;G,T)
Alt rs137854656(G,T;G,T)
Reference rs137854656(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324670G>A; NC_000006.11:g.31324670G>C
CLNSRC
CLNACC