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rs151341095

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341095(C;T)
Make rs151341095(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356927
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341095
ebirs151341095
HLIrs151341095
Exacrs151341095
Varsomers151341095
Maprs151341095
PheGenIrs151341095
hapmaprs151341095
1000 genomesrs151341095
hgdprs151341095
ensemblrs151341095
gopubmedrs151341095
geneviewrs151341095
scholarrs151341095
googlers151341095
pharmgkbrs151341095
gwascentralrs151341095
openSNPrs151341095
23andMers151341095
23andMe allrs151341095
SNP Nexus

SNPshotrs151341095
SNPdbers151341095
MSV3drs151341095
GWAS Ctlgrs151341095
Max Magnitude0
ClinVar
Risk rs151341095(T;T)
Alt rs151341095(T;T)
Reference rs151341095(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324704G>A
CLNSRC
CLNACC