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rs151341148

From SNPedia

Merged intors151341147
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341148(C;C)
Make rs151341148(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356806
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341148
ebirs151341148
HLIrs151341148
Exacrs151341148
Varsomers151341148
Maprs151341148
PheGenIrs151341148
hapmaprs151341148
1000 genomesrs151341148
hgdprs151341148
ensemblrs151341148
gopubmedrs151341148
geneviewrs151341148
scholarrs151341148
googlers151341148
pharmgkbrs151341148
gwascentralrs151341148
openSNPrs151341148
23andMers151341148
23andMe allrs151341148
SNP Nexus

SNPshotrs151341148
SNPdbers151341148
MSV3drs151341148
GWAS Ctlgrs151341148
StatusMerged into rs151341147
Max Magnitude0
ClinVar
Risk rs151341148(C;C)
Alt rs151341148(C;C)
Reference rs151341148(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324583C>G
CLNSRC
CLNACC