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rs151341199

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341199(C;C)
Make rs151341199(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356706
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341199
ebirs151341199
HLIrs151341199
Exacrs151341199
Varsomers151341199
Maprs151341199
PheGenIrs151341199
hapmaprs151341199
1000 genomesrs151341199
hgdprs151341199
ensemblrs151341199
gopubmedrs151341199
geneviewrs151341199
scholarrs151341199
googlers151341199
pharmgkbrs151341199
gwascentralrs151341199
openSNPrs151341199
23andMers151341199
23andMe allrs151341199
SNP Nexus

SNPshotrs151341199
SNPdbers151341199
MSV3drs151341199
GWAS Ctlgrs151341199
Max Magnitude0
ClinVar
Risk rs151341199(C;C)
Alt rs151341199(C;C)
Reference rs151341199(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324483A>G
CLNSRC
CLNACC