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rs151341264

From SNPedia

Merged intors151341262
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341264(C;T)
Make rs151341264(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356293
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341264
ebirs151341264
HLIrs151341264
Exacrs151341264
Varsomers151341264
Maprs151341264
PheGenIrs151341264
hapmaprs151341264
1000 genomesrs151341264
hgdprs151341264
ensemblrs151341264
gopubmedrs151341264
geneviewrs151341264
scholarrs151341264
googlers151341264
pharmgkbrs151341264
gwascentralrs151341264
openSNPrs151341264
23andMers151341264
23andMe allrs151341264
SNP Nexus

SNPshotrs151341264
SNPdbers151341264
MSV3drs151341264
GWAS Ctlgrs151341264
StatusMerged into rs151341262
Max Magnitude0
ClinVar
Risk rs151341264(T;T)
Alt rs151341264(T;T)
Reference rs151341264(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324070G>A
CLNSRC
CLNACC