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rs151341288

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341288(A;G)
Make rs151341288(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356271
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341288
ebirs151341288
HLIrs151341288
Exacrs151341288
Varsomers151341288
Maprs151341288
PheGenIrs151341288
hapmaprs151341288
1000 genomesrs151341288
hgdprs151341288
ensemblrs151341288
gopubmedrs151341288
geneviewrs151341288
scholarrs151341288
googlers151341288
pharmgkbrs151341288
gwascentralrs151341288
openSNPrs151341288
23andMers151341288
23andMe allrs151341288
SNP Nexus

SNPshotrs151341288
SNPdbers151341288
MSV3drs151341288
GWAS Ctlgrs151341288
Max Magnitude0
ClinVar
Risk rs151341288(G;G)
Alt rs151341288(G;G)
Reference rs151341288(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324048T>C
CLNSRC
CLNACC