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rs151341280

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341280(A;A)
Make rs151341280(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356284
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341280
ebirs151341280
HLIrs151341280
Exacrs151341280
Varsomers151341280
Maprs151341280
PheGenIrs151341280
hapmaprs151341280
1000 genomesrs151341280
hgdprs151341280
ensemblrs151341280
gopubmedrs151341280
geneviewrs151341280
scholarrs151341280
googlers151341280
pharmgkbrs151341280
gwascentralrs151341280
openSNPrs151341280
23andMers151341280
23andMe allrs151341280
SNP Nexus

SNPshotrs151341280
SNPdbers151341280
MSV3drs151341280
GWAS Ctlgrs151341280
Merged fromRs151341281
Max Magnitude0
ClinVar
Risk rs151341280(A,T;A,T)
Alt rs151341280(A,T;A,T)
Reference rs151341280(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324061G>A; NC_000006.11:g.31324061G>T
CLNSRC
CLNACC