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rs137854671

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854671(C;G)
Make rs137854671(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356839
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854671
ebirs137854671
HLIrs137854671
Exacrs137854671
Varsomers137854671
Maprs137854671
PheGenIrs137854671
hapmaprs137854671
1000 genomesrs137854671
hgdprs137854671
ensemblrs137854671
gopubmedrs137854671
geneviewrs137854671
scholarrs137854671
googlers137854671
pharmgkbrs137854671
gwascentralrs137854671
openSNPrs137854671
23andMers137854671
23andMe allrs137854671
SNP Nexus

SNPshotrs137854671
SNPdbers137854671
MSV3drs137854671
GWAS Ctlgrs137854671
Max Magnitude0
ClinVar
Risk rs137854671(G,T;G,T)
Alt rs137854671(G,T;G,T)
Reference rs137854671(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324616G>A; NC_000006.11:g.31324616G>C
CLNSRC
CLNACC