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rs151341291

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341291(A;A)
Make rs151341291(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356266
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341291
ebirs151341291
HLIrs151341291
Exacrs151341291
Varsomers151341291
Maprs151341291
PheGenIrs151341291
hapmaprs151341291
1000 genomesrs151341291
hgdprs151341291
ensemblrs151341291
gopubmedrs151341291
geneviewrs151341291
scholarrs151341291
googlers151341291
pharmgkbrs151341291
gwascentralrs151341291
openSNPrs151341291
23andMers151341291
23andMe allrs151341291
SNP Nexus

SNPshotrs151341291
SNPdbers151341291
MSV3drs151341291
GWAS Ctlgrs151341291
Max Magnitude0
ClinVar
Risk rs151341291(A;A)
Alt rs151341291(A;A)
Reference rs151341291(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324043C>T
CLNSRC
CLNACC