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rs137854729

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137854729(A;G)
Make rs137854729(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356349
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854729
ebirs137854729
HLIrs137854729
Exacrs137854729
Varsomers137854729
Maprs137854729
PheGenIrs137854729
hapmaprs137854729
1000 genomesrs137854729
hgdprs137854729
ensemblrs137854729
gopubmedrs137854729
geneviewrs137854729
scholarrs137854729
googlers137854729
pharmgkbrs137854729
gwascentralrs137854729
openSNPrs137854729
23andMers137854729
23andMe allrs137854729
SNP Nexus

SNPshotrs137854729
SNPdbers137854729
MSV3drs137854729
GWAS Ctlgrs137854729
Max Magnitude0
ClinVar
Risk rs137854729(G,T;G,T)
Alt rs137854729(G,T;G,T)
Reference rs137854729(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324126T>A; NC_000006.11:g.31324126T>C
CLNSRC
CLNACC