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rs151341290

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341290(C;C)
Make rs151341290(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356267
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341290
ebirs151341290
HLIrs151341290
Exacrs151341290
Varsomers151341290
Maprs151341290
PheGenIrs151341290
hapmaprs151341290
1000 genomesrs151341290
hgdprs151341290
ensemblrs151341290
gopubmedrs151341290
geneviewrs151341290
scholarrs151341290
googlers151341290
pharmgkbrs151341290
gwascentralrs151341290
openSNPrs151341290
23andMers151341290
23andMe allrs151341290
SNP Nexus

SNPshotrs151341290
SNPdbers151341290
MSV3drs151341290
GWAS Ctlgrs151341290
Max Magnitude0
ClinVar
Risk rs151341290(C;C)
Alt rs151341290(C;C)
Reference rs151341290(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324044C>G
CLNSRC
CLNACC