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rs151341234

From SNPedia

Merged intors151341233
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341234(C;C)
Make rs151341234(C;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324159
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341234
ebirs151341234
HLIrs151341234
Exacrs151341234
Varsomers151341234
Maprs151341234
PheGenIrs151341234
hapmaprs151341234
1000 genomesrs151341234
hgdprs151341234
ensemblrs151341234
gopubmedrs151341234
geneviewrs151341234
scholarrs151341234
googlers151341234
pharmgkbrs151341234
gwascentralrs151341234
openSNPrs151341234
23andMers151341234
23andMe allrs151341234
SNP Nexus

SNPshotrs151341234
SNPdbers151341234
MSV3drs151341234
GWAS Ctlgrs151341234
StatusMerged into rs151341233
Max Magnitude0
ClinVar
Risk rs151341234(C;C)
Alt rs151341234(C;C)
Reference rs151341234(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324159C>G
CLNSRC
CLNACC