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rs137854713

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854713(C;C)
Make rs137854713(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356395
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854713
ebirs137854713
HLIrs137854713
Exacrs137854713
Varsomers137854713
Maprs137854713
PheGenIrs137854713
hapmaprs137854713
1000 genomesrs137854713
hgdprs137854713
ensemblrs137854713
gopubmedrs137854713
geneviewrs137854713
scholarrs137854713
googlers137854713
pharmgkbrs137854713
gwascentralrs137854713
openSNPrs137854713
23andMers137854713
23andMe allrs137854713
SNP Nexus

SNPshotrs137854713
SNPdbers137854713
MSV3drs137854713
GWAS Ctlgrs137854713
Max Magnitude0
ClinVar
Risk rs137854713(C,T;C,T)
Alt rs137854713(C,T;C,T)
Reference rs137854713(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324172C>A; NC_000006.11:g.31324172C>G
CLNSRC
CLNACC