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rs151341393

From SNPedia

Merged intors3819290
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341393(C;T)
Make rs151341393(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354885
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341393
ebirs151341393
HLIrs151341393
Exacrs151341393
Varsomers151341393
Maprs151341393
PheGenIrs151341393
hapmaprs151341393
1000 genomesrs151341393
hgdprs151341393
ensemblrs151341393
gopubmedrs151341393
geneviewrs151341393
scholarrs151341393
googlers151341393
pharmgkbrs151341393
gwascentralrs151341393
openSNPrs151341393
23andMers151341393
23andMe allrs151341393
SNP Nexus

SNPshotrs151341393
SNPdbers151341393
MSV3drs151341393
GWAS Ctlgrs151341393
StatusMerged into rs3819290
Max Magnitude0
ClinVar
Risk rs151341393(T;T)
Alt rs151341393(T;T)
Reference rs151341393(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322662G>A
CLNSRC
CLNACC