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rs151341153

From SNPedia

Merged intors151341152
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341153(G;G)
Make rs151341153(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356804
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341153
ebirs151341153
HLIrs151341153
Exacrs151341153
Varsomers151341153
Maprs151341153
PheGenIrs151341153
hapmaprs151341153
1000 genomesrs151341153
hgdprs151341153
ensemblrs151341153
gopubmedrs151341153
geneviewrs151341153
scholarrs151341153
googlers151341153
pharmgkbrs151341153
gwascentralrs151341153
openSNPrs151341153
23andMers151341153
23andMe allrs151341153
SNP Nexus

SNPshotrs151341153
SNPdbers151341153
MSV3drs151341153
GWAS Ctlgrs151341153
StatusMerged into rs151341152
Max Magnitude0
ClinVar
Risk rs151341153(G;G)
Alt rs151341153(G;G)
Reference rs151341153(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324581A>C
CLNSRC
CLNACC