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rs137854774

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854774(A;A)
Make rs137854774(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356205
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854774
ebirs137854774
HLIrs137854774
Exacrs137854774
Varsomers137854774
Maprs137854774
PheGenIrs137854774
hapmaprs137854774
1000 genomesrs137854774
hgdprs137854774
ensemblrs137854774
gopubmedrs137854774
geneviewrs137854774
scholarrs137854774
googlers137854774
pharmgkbrs137854774
gwascentralrs137854774
openSNPrs137854774
23andMers137854774
23andMe allrs137854774
SNP Nexus

SNPshotrs137854774
SNPdbers137854774
MSV3drs137854774
GWAS Ctlgrs137854774
Max Magnitude0
ClinVar
Risk rs137854774(A;A) rs137854774(C;C)
Alt rs137854774(A;A) rs137854774(C;C)
Reference Rs137854774(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323982C>G; NC_000006.11:g.31323982C>T
CLNSRC
CLNACC