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rs137854755

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854755(A;A)
Make rs137854755(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356268
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854755
ebirs137854755
HLIrs137854755
Exacrs137854755
Varsomers137854755
Maprs137854755
PheGenIrs137854755
hapmaprs137854755
1000 genomesrs137854755
hgdprs137854755
ensemblrs137854755
gopubmedrs137854755
geneviewrs137854755
scholarrs137854755
googlers137854755
pharmgkbrs137854755
gwascentralrs137854755
openSNPrs137854755
23andMers137854755
23andMe allrs137854755
SNP Nexus

SNPshotrs137854755
SNPdbers137854755
MSV3drs137854755
GWAS Ctlgrs137854755
Max Magnitude0
ClinVar
Risk rs137854755(A,G;A,G)
Alt rs137854755(A,G;A,G)
Reference rs137854755(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324045G>C; NC_000006.11:g.31324045G>T
CLNSRC
CLNACC