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rs151341073

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341073(C;T)
Make rs151341073(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357224
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341073
ebirs151341073
HLIrs151341073
Exacrs151341073
Varsomers151341073
Maprs151341073
PheGenIrs151341073
hapmaprs151341073
1000 genomesrs151341073
hgdprs151341073
ensemblrs151341073
gopubmedrs151341073
geneviewrs151341073
scholarrs151341073
googlers151341073
pharmgkbrs151341073
gwascentralrs151341073
openSNPrs151341073
23andMers151341073
23andMe allrs151341073
SNP Nexus

SNPshotrs151341073
SNPdbers151341073
MSV3drs151341073
GWAS Ctlgrs151341073
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs151341073(T;T)
Alt rs151341073(T;T)
Reference rs151341073(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31325001G>A
CLNSRC
CLNACC