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rs151341323

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341323(C;T)
Make rs151341323(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356207
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341323
ebirs151341323
HLIrs151341323
Exacrs151341323
Varsomers151341323
Maprs151341323
PheGenIrs151341323
hapmaprs151341323
1000 genomesrs151341323
hgdprs151341323
ensemblrs151341323
gopubmedrs151341323
geneviewrs151341323
scholarrs151341323
googlers151341323
pharmgkbrs151341323
gwascentralrs151341323
openSNPrs151341323
23andMers151341323
23andMe allrs151341323
SNP Nexus

SNPshotrs151341323
SNPdbers151341323
MSV3drs151341323
GWAS Ctlgrs151341323
Max Magnitude0
ClinVar
Risk rs151341323(T;T)
Alt rs151341323(T;T)
Reference rs151341323(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323984G>A
CLNSRC
CLNACC