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rs137854772

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854772(A;A)
Make rs137854772(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356208
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854772
ebirs137854772
HLIrs137854772
Exacrs137854772
Varsomers137854772
Maprs137854772
PheGenIrs137854772
hapmaprs137854772
1000 genomesrs137854772
hgdprs137854772
ensemblrs137854772
gopubmedrs137854772
geneviewrs137854772
scholarrs137854772
googlers137854772
pharmgkbrs137854772
gwascentralrs137854772
openSNPrs137854772
23andMers137854772
23andMe allrs137854772
SNP Nexus

SNPshotrs137854772
SNPdbers137854772
MSV3drs137854772
GWAS Ctlgrs137854772
Max Magnitude0
ClinVar
Risk rs137854772(A,T;A,T)
Alt rs137854772(A,T;A,T)
Reference rs137854772(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323985C>A; NC_000006.11:g.31323985C>T
CLNSRC
CLNACC