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rs151341203

From SNPedia

Merged intors151341201
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341203(C;T)
Make rs151341203(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356704
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341203
ebirs151341203
HLIrs151341203
Exacrs151341203
Varsomers151341203
Maprs151341203
PheGenIrs151341203
hapmaprs151341203
1000 genomesrs151341203
hgdprs151341203
ensemblrs151341203
gopubmedrs151341203
geneviewrs151341203
scholarrs151341203
googlers151341203
pharmgkbrs151341203
gwascentralrs151341203
openSNPrs151341203
23andMers151341203
23andMe allrs151341203
SNP Nexus

SNPshotrs151341203
SNPdbers151341203
MSV3drs151341203
GWAS Ctlgrs151341203
StatusMerged into rs151341201
Max Magnitude0
ClinVar
Risk rs151341203(T;T)
Alt rs151341203(T;T)
Reference rs151341203(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324481G>A
CLNSRC
CLNACC