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rs151341277

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341277(C;T)
Make rs151341277(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356285
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341277
ebirs151341277
HLIrs151341277
Exacrs151341277
Varsomers151341277
Maprs151341277
PheGenIrs151341277
hapmaprs151341277
1000 genomesrs151341277
hgdprs151341277
ensemblrs151341277
gopubmedrs151341277
geneviewrs151341277
scholarrs151341277
googlers151341277
pharmgkbrs151341277
gwascentralrs151341277
openSNPrs151341277
23andMers151341277
23andMe allrs151341277
SNP Nexus

SNPshotrs151341277
SNPdbers151341277
MSV3drs151341277
GWAS Ctlgrs151341277
Merged fromRs151341278
Max Magnitude0
ClinVar
Risk rs151341277(G,T;G,T)
Alt rs151341277(G,T;G,T)
Reference rs151341277(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324062G>A; NC_000006.11:g.31324062G>C
CLNSRC
CLNACC