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rs151341096

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341096(C;C)
Make rs151341096(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356923
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341096
ebirs151341096
HLIrs151341096
Exacrs151341096
Varsomers151341096
Maprs151341096
PheGenIrs151341096
hapmaprs151341096
1000 genomesrs151341096
hgdprs151341096
ensemblrs151341096
gopubmedrs151341096
geneviewrs151341096
scholarrs151341096
googlers151341096
pharmgkbrs151341096
gwascentralrs151341096
openSNPrs151341096
23andMers151341096
23andMe allrs151341096
SNP Nexus

SNPshotrs151341096
SNPdbers151341096
MSV3drs151341096
GWAS Ctlgrs151341096
Max Magnitude0
ClinVar
Risk rs151341096(A,C;A,C)
Alt rs151341096(A,C;A,C)
Reference rs151341096(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324700C>G; NC_000006.11:g.31324700C>T
CLNSRC
CLNACC