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rs151341289

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341289(C;C)
Make rs151341289(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356270
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341289
ebirs151341289
HLIrs151341289
Exacrs151341289
Varsomers151341289
Maprs151341289
PheGenIrs151341289
hapmaprs151341289
1000 genomesrs151341289
hgdprs151341289
ensemblrs151341289
gopubmedrs151341289
geneviewrs151341289
scholarrs151341289
googlers151341289
pharmgkbrs151341289
gwascentralrs151341289
openSNPrs151341289
23andMers151341289
23andMe allrs151341289
SNP Nexus

SNPshotrs151341289
SNPdbers151341289
MSV3drs151341289
GWAS Ctlgrs151341289
Max Magnitude0
ClinVar
Risk rs151341289(C;C)
Alt rs151341289(C;C)
Reference rs151341289(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324047C>G
CLNSRC
CLNACC