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rs151341299

From SNPedia

Merged intors151341297
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341299(G;T)
Make rs151341299(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356258
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341299
ebirs151341299
HLIrs151341299
Exacrs151341299
Varsomers151341299
Maprs151341299
PheGenIrs151341299
hapmaprs151341299
1000 genomesrs151341299
hgdprs151341299
ensemblrs151341299
gopubmedrs151341299
geneviewrs151341299
scholarrs151341299
googlers151341299
pharmgkbrs151341299
gwascentralrs151341299
openSNPrs151341299
23andMers151341299
23andMe allrs151341299
SNP Nexus

SNPshotrs151341299
SNPdbers151341299
MSV3drs151341299
GWAS Ctlgrs151341299
StatusMerged into rs151341297
Max Magnitude0
ClinVar
Risk rs151341299(T;T)
Alt rs151341299(T;T)
Reference rs151341299(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324035C>A
CLNSRC
CLNACC