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rs151341151

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341151(-;-)
Make rs151341151(-;T)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324581
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341151
ebirs151341151
HLIrs151341151
Exacrs151341151
Varsomers151341151
Maprs151341151
PheGenIrs151341151
hapmaprs151341151
1000 genomesrs151341151
hgdprs151341151
ensemblrs151341151
gopubmedrs151341151
geneviewrs151341151
scholarrs151341151
googlers151341151
pharmgkbrs151341151
gwascentralrs151341151
openSNPrs151341151
23andMers151341151
23andMe allrs151341151
SNP Nexus

SNPshotrs151341151
SNPdbers151341151
MSV3drs151341151
GWAS Ctlgrs151341151
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341151(;)
Alt rs151341151(;)
Reference rs151341151(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324581delA
CLNSRC
CLNACC