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rs151341075

From SNPedia

Merged intors9266206
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341075(G;G)
Make rs151341075(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357154
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341075
ebirs151341075
HLIrs151341075
Exacrs151341075
Varsomers151341075
Maprs151341075
PheGenIrs151341075
hapmaprs151341075
1000 genomesrs151341075
hgdprs151341075
ensemblrs151341075
gopubmedrs151341075
geneviewrs151341075
scholarrs151341075
googlers151341075
pharmgkbrs151341075
gwascentralrs151341075
openSNPrs151341075
23andMers151341075
23andMe allrs151341075
SNP Nexus

SNPshotrs151341075
SNPdbers151341075
MSV3drs151341075
GWAS Ctlgrs151341075
StatusMerged into rs9266206
Max Magnitude0
ClinVar
Risk rs151341075(G;G)
Alt rs151341075(G;G)
Reference rs151341075(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324931A>C
CLNSRC
CLNACC