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rs151341322

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341322(C;C)
Make rs151341322(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356211
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341322
ebirs151341322
HLIrs151341322
Exacrs151341322
Varsomers151341322
Maprs151341322
PheGenIrs151341322
hapmaprs151341322
1000 genomesrs151341322
hgdprs151341322
ensemblrs151341322
gopubmedrs151341322
geneviewrs151341322
scholarrs151341322
googlers151341322
pharmgkbrs151341322
gwascentralrs151341322
openSNPrs151341322
23andMers151341322
23andMe allrs151341322
SNP Nexus

SNPshotrs151341322
SNPdbers151341322
MSV3drs151341322
GWAS Ctlgrs151341322
Max Magnitude0
ClinVar
Risk rs151341322(C,G;C,G)
Alt rs151341322(C,G;C,G)
Reference rs151341322(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323988A>C; NC_000006.11:g.31323988A>G
CLNSRC
CLNACC