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rs151341190

From SNPedia

Merged intors151341189
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341190(G;T)
Make rs151341190(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356764
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341190
ebirs151341190
HLIrs151341190
Exacrs151341190
Varsomers151341190
Maprs151341190
PheGenIrs151341190
hapmaprs151341190
1000 genomesrs151341190
hgdprs151341190
ensemblrs151341190
gopubmedrs151341190
geneviewrs151341190
scholarrs151341190
googlers151341190
pharmgkbrs151341190
gwascentralrs151341190
openSNPrs151341190
23andMers151341190
23andMe allrs151341190
SNP Nexus

SNPshotrs151341190
SNPdbers151341190
MSV3drs151341190
GWAS Ctlgrs151341190
StatusMerged into rs151341189
Max Magnitude0
ClinVar
Risk rs151341190(T;T)
Alt rs151341190(T;T)
Reference rs151341190(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324541C>A
CLNSRC
CLNACC