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rs137854719

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854719(C;G)
Make rs137854719(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356383
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854719
ebirs137854719
HLIrs137854719
Exacrs137854719
Varsomers137854719
Maprs137854719
PheGenIrs137854719
hapmaprs137854719
1000 genomesrs137854719
hgdprs137854719
ensemblrs137854719
gopubmedrs137854719
geneviewrs137854719
scholarrs137854719
googlers137854719
pharmgkbrs137854719
gwascentralrs137854719
openSNPrs137854719
23andMers137854719
23andMe allrs137854719
SNP Nexus

SNPshotrs137854719
SNPdbers137854719
MSV3drs137854719
GWAS Ctlgrs137854719
Max Magnitude0
ClinVar
Risk rs137854719(G,T;G,T)
Alt rs137854719(G,T;G,T)
Reference rs137854719(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324160G>A; NC_000006.11:g.31324160G>C
CLNSRC
CLNACC