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rs151341275

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341275(C;T)
Make rs151341275(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356286
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341275
ebirs151341275
HLIrs151341275
Exacrs151341275
Varsomers151341275
Maprs151341275
PheGenIrs151341275
hapmaprs151341275
1000 genomesrs151341275
hgdprs151341275
ensemblrs151341275
gopubmedrs151341275
geneviewrs151341275
scholarrs151341275
googlers151341275
pharmgkbrs151341275
gwascentralrs151341275
openSNPrs151341275
23andMers151341275
23andMe allrs151341275
SNP Nexus

SNPshotrs151341275
SNPdbers151341275
MSV3drs151341275
GWAS Ctlgrs151341275
Max Magnitude0
ClinVar
Risk rs151341275(T;T)
Alt rs151341275(T;T)
Reference rs151341275(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324063G>A
CLNSRC
CLNACC