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rs151341313

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341313(C;T)
Make rs151341313(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356237
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341313
ebirs151341313
HLIrs151341313
Exacrs151341313
Varsomers151341313
Maprs151341313
PheGenIrs151341313
hapmaprs151341313
1000 genomesrs151341313
hgdprs151341313
ensemblrs151341313
gopubmedrs151341313
geneviewrs151341313
scholarrs151341313
googlers151341313
pharmgkbrs151341313
gwascentralrs151341313
openSNPrs151341313
23andMers151341313
23andMe allrs151341313
SNP Nexus

SNPshotrs151341313
SNPdbers151341313
MSV3drs151341313
GWAS Ctlgrs151341313
Max Magnitude0
ClinVar
Risk rs151341313(A,T;A,T)
Alt rs151341313(A,T;A,T)
Reference rs151341313(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324014G>A; NC_000006.11:g.31324014G>T
CLNSRC
CLNACC