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rs137854786

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137854786(A;A)
Make rs137854786(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356178
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854786
ebirs137854786
HLIrs137854786
Exacrs137854786
Varsomers137854786
Maprs137854786
PheGenIrs137854786
hapmaprs137854786
1000 genomesrs137854786
hgdprs137854786
ensemblrs137854786
gopubmedrs137854786
geneviewrs137854786
scholarrs137854786
googlers137854786
pharmgkbrs137854786
gwascentralrs137854786
openSNPrs137854786
23andMers137854786
23andMe allrs137854786
SNP Nexus

SNPshotrs137854786
SNPdbers137854786
MSV3drs137854786
GWAS Ctlgrs137854786
Max Magnitude0
ClinVar
Risk rs137854786(A,G;A,G)
Alt rs137854786(A,G;A,G)
Reference rs137854786(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323955A>C; NC_000006.11:g.31323955A>T
CLNSRC
CLNACC