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rs137854715

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854715(A;A)
Make rs137854715(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356392
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854715
ebirs137854715
HLIrs137854715
Exacrs137854715
Varsomers137854715
Maprs137854715
PheGenIrs137854715
hapmaprs137854715
1000 genomesrs137854715
hgdprs137854715
ensemblrs137854715
gopubmedrs137854715
geneviewrs137854715
scholarrs137854715
googlers137854715
pharmgkbrs137854715
gwascentralrs137854715
openSNPrs137854715
23andMers137854715
23andMe allrs137854715
SNP Nexus

SNPshotrs137854715
SNPdbers137854715
MSV3drs137854715
GWAS Ctlgrs137854715
Max Magnitude0
ClinVar
Risk rs137854715(A,T;A,T)
Alt rs137854715(A,T;A,T)
Reference rs137854715(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324169G>A; NC_000006.11:g.31324169G>T
CLNSRC
CLNACC