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rs137854846

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854846(C;C)
Make rs137854846(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354434
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854846
ebirs137854846
HLIrs137854846
Exacrs137854846
Varsomers137854846
Maprs137854846
PheGenIrs137854846
hapmaprs137854846
1000 genomesrs137854846
hgdprs137854846
ensemblrs137854846
gopubmedrs137854846
geneviewrs137854846
scholarrs137854846
googlers137854846
pharmgkbrs137854846
gwascentralrs137854846
openSNPrs137854846
23andMers137854846
23andMe allrs137854846
SNP Nexus

SNPshotrs137854846
SNPdbers137854846
MSV3drs137854846
GWAS Ctlgrs137854846
Max Magnitude0
ClinVar
Risk rs137854846(C,T;C,T)
Alt rs137854846(C,T;C,T)
Reference rs137854846(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322211C>A; NC_000006.11:g.31322211C>G
CLNSRC
CLNACC