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rs137854727

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854727(C;C)
Make rs137854727(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356359
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854727
ebirs137854727
HLIrs137854727
Exacrs137854727
Varsomers137854727
Maprs137854727
PheGenIrs137854727
hapmaprs137854727
1000 genomesrs137854727
hgdprs137854727
ensemblrs137854727
gopubmedrs137854727
geneviewrs137854727
scholarrs137854727
googlers137854727
pharmgkbrs137854727
gwascentralrs137854727
openSNPrs137854727
23andMers137854727
23andMe allrs137854727
SNP Nexus

SNPshotrs137854727
SNPdbers137854727
MSV3drs137854727
GWAS Ctlgrs137854727
Max Magnitude0
ClinVar
Risk rs137854727(A,C,T;A,C,T)
Alt rs137854727(A,C,T;A,C,T)
Reference rs137854727(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324136C>A; NC_000006.11:g.31324136C>G; NC_000006.11:g.31324136C>T
CLNSRC
CLNACC