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rs151341285

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341285(C;T)
Make rs151341285(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356279
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341285
ebirs151341285
HLIrs151341285
Exacrs151341285
Varsomers151341285
Maprs151341285
PheGenIrs151341285
hapmaprs151341285
1000 genomesrs151341285
hgdprs151341285
ensemblrs151341285
gopubmedrs151341285
geneviewrs151341285
scholarrs151341285
googlers151341285
pharmgkbrs151341285
gwascentralrs151341285
openSNPrs151341285
23andMers151341285
23andMe allrs151341285
SNP Nexus

SNPshotrs151341285
SNPdbers151341285
MSV3drs151341285
GWAS Ctlgrs151341285
Max Magnitude0
ClinVar
Risk rs151341285(T;T)
Alt rs151341285(T;T)
Reference rs151341285(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324056G>A
CLNSRC
CLNACC