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rs151341333

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341333(C;C)
Make rs151341333(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356180
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341333
ebirs151341333
HLIrs151341333
Exacrs151341333
Varsomers151341333
Maprs151341333
PheGenIrs151341333
hapmaprs151341333
1000 genomesrs151341333
hgdprs151341333
ensemblrs151341333
gopubmedrs151341333
geneviewrs151341333
scholarrs151341333
googlers151341333
pharmgkbrs151341333
gwascentralrs151341333
openSNPrs151341333
23andMers151341333
23andMe allrs151341333
SNP Nexus

SNPshotrs151341333
SNPdbers151341333
MSV3drs151341333
GWAS Ctlgrs151341333
Max Magnitude0
ClinVar
Risk rs151341333(C;C)
Alt rs151341333(C;C)
Reference rs151341333(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323957C>G
CLNSRC
CLNACC