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rs151341356

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341356(A;A)
Make rs151341356(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355393
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341356
ebirs151341356
HLIrs151341356
Exacrs151341356
Varsomers151341356
Maprs151341356
PheGenIrs151341356
hapmaprs151341356
1000 genomesrs151341356
hgdprs151341356
ensemblrs151341356
gopubmedrs151341356
geneviewrs151341356
scholarrs151341356
googlers151341356
pharmgkbrs151341356
gwascentralrs151341356
openSNPrs151341356
23andMers151341356
23andMe allrs151341356
SNP Nexus

SNPshotrs151341356
SNPdbers151341356
MSV3drs151341356
GWAS Ctlgrs151341356
Max Magnitude0
ClinVar
Risk rs151341356(A;A)
Alt rs151341356(A;A)
Reference rs151341356(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323170C>T
CLNSRC
CLNACC