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rs151341103

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341103(C;T)
Make rs151341103(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356908
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341103
ebirs151341103
HLIrs151341103
Exacrs151341103
Varsomers151341103
Maprs151341103
PheGenIrs151341103
hapmaprs151341103
1000 genomesrs151341103
hgdprs151341103
ensemblrs151341103
gopubmedrs151341103
geneviewrs151341103
scholarrs151341103
googlers151341103
pharmgkbrs151341103
gwascentralrs151341103
openSNPrs151341103
23andMers151341103
23andMe allrs151341103
SNP Nexus

SNPshotrs151341103
SNPdbers151341103
MSV3drs151341103
GWAS Ctlgrs151341103
Max Magnitude0
ClinVar
Risk rs151341103(T;T)
Alt rs151341103(T;T)
Reference rs151341103(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324685G>A
CLNSRC
CLNACC