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rs137854711

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854711(A;A)
Make rs137854711(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356402
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854711
ebirs137854711
HLIrs137854711
Exacrs137854711
Varsomers137854711
Maprs137854711
PheGenIrs137854711
hapmaprs137854711
1000 genomesrs137854711
hgdprs137854711
ensemblrs137854711
gopubmedrs137854711
geneviewrs137854711
scholarrs137854711
googlers137854711
pharmgkbrs137854711
gwascentralrs137854711
openSNPrs137854711
23andMers137854711
23andMe allrs137854711
SNP Nexus

SNPshotrs137854711
SNPdbers137854711
MSV3drs137854711
GWAS Ctlgrs137854711
Max Magnitude0
ClinVar
Risk rs137854711(A,T;A,T)
Alt rs137854711(A,T;A,T)
Reference rs137854711(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324179C>A; NC_000006.11:g.31324179C>T
CLNSRC
CLNACC