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rs151341189

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341189(A;A)
Make rs151341189(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356764
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341189
ebirs151341189
HLIrs151341189
Exacrs151341189
Varsomers151341189
Maprs151341189
PheGenIrs151341189
hapmaprs151341189
1000 genomesrs151341189
hgdprs151341189
ensemblrs151341189
gopubmedrs151341189
geneviewrs151341189
scholarrs151341189
googlers151341189
pharmgkbrs151341189
gwascentralrs151341189
openSNPrs151341189
23andMers151341189
23andMe allrs151341189
SNP Nexus

SNPshotrs151341189
SNPdbers151341189
MSV3drs151341189
GWAS Ctlgrs151341189
Merged fromRs151341190
Max Magnitude0
ClinVar
Risk rs151341189(A,T;A,T)
Alt rs151341189(A,T;A,T)
Reference rs151341189(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324541C>A; NC_000006.11:g.31324541C>T
CLNSRC
CLNACC