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rs151341233

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341233(C;C)
Make rs151341233(C;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324159
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341233
ebirs151341233
HLIrs151341233
Exacrs151341233
Varsomers151341233
Maprs151341233
PheGenIrs151341233
hapmaprs151341233
1000 genomesrs151341233
hgdprs151341233
ensemblrs151341233
gopubmedrs151341233
geneviewrs151341233
scholarrs151341233
googlers151341233
pharmgkbrs151341233
gwascentralrs151341233
openSNPrs151341233
23andMers151341233
23andMe allrs151341233
SNP Nexus

SNPshotrs151341233
SNPdbers151341233
MSV3drs151341233
GWAS Ctlgrs151341233
StatusDeleted
Merged fromRs151341234, Rs151341235
Max Magnitude0
ClinVar
Risk rs151341233(A;A)
Alt rs151341233(A;A)
Reference rs151341233(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324159C>T
CLNSRC
CLNACC