Have questions? Visit https://www.reddit.com/r/SNPedia

rs151341298

From SNPedia

Merged intors151341297
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341298(C;C)
Make rs151341298(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356258
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341298
ebirs151341298
HLIrs151341298
Exacrs151341298
Varsomers151341298
Maprs151341298
PheGenIrs151341298
hapmaprs151341298
1000 genomesrs151341298
hgdprs151341298
ensemblrs151341298
gopubmedrs151341298
geneviewrs151341298
scholarrs151341298
googlers151341298
pharmgkbrs151341298
gwascentralrs151341298
openSNPrs151341298
23andMers151341298
23andMe allrs151341298
SNP Nexus

SNPshotrs151341298
SNPdbers151341298
MSV3drs151341298
GWAS Ctlgrs151341298
StatusMerged into rs151341297
Max Magnitude0
ClinVar
Risk rs151341298(C;C)
Alt rs151341298(C;C)
Reference rs151341298(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324035C>G
CLNSRC
CLNACC