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rs151341247

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341247(C;C)
Make rs151341247(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356317
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341247
ebirs151341247
HLIrs151341247
Exacrs151341247
Varsomers151341247
Maprs151341247
PheGenIrs151341247
hapmaprs151341247
1000 genomesrs151341247
hgdprs151341247
ensemblrs151341247
gopubmedrs151341247
geneviewrs151341247
scholarrs151341247
googlers151341247
pharmgkbrs151341247
gwascentralrs151341247
openSNPrs151341247
23andMers151341247
23andMe allrs151341247
SNP Nexus

SNPshotrs151341247
SNPdbers151341247
MSV3drs151341247
GWAS Ctlgrs151341247
Max Magnitude0
ClinVar
Risk rs151341247(C;C)
Alt rs151341247(C;C)
Reference rs151341247(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324094A>G
CLNSRC
CLNACC