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rs137854747

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854747(A;A)
Make rs137854747(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356282
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854747
ebirs137854747
HLIrs137854747
Exacrs137854747
Varsomers137854747
Maprs137854747
PheGenIrs137854747
hapmaprs137854747
1000 genomesrs137854747
hgdprs137854747
ensemblrs137854747
gopubmedrs137854747
geneviewrs137854747
scholarrs137854747
googlers137854747
pharmgkbrs137854747
gwascentralrs137854747
openSNPrs137854747
23andMers137854747
23andMe allrs137854747
SNP Nexus

SNPshotrs137854747
SNPdbers137854747
MSV3drs137854747
GWAS Ctlgrs137854747
Max Magnitude0
ClinVar
Risk rs137854747(A,C;A,C)
Alt rs137854747(A,C;A,C)
Reference rs137854747(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324059C>G; NC_000006.11:g.31324059C>T
CLNSRC
CLNACC