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rs151341329

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341329(C;C)
Make rs151341329(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356189
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341329
ebirs151341329
HLIrs151341329
Exacrs151341329
Varsomers151341329
Maprs151341329
PheGenIrs151341329
hapmaprs151341329
1000 genomesrs151341329
hgdprs151341329
ensemblrs151341329
gopubmedrs151341329
geneviewrs151341329
scholarrs151341329
googlers151341329
pharmgkbrs151341329
gwascentralrs151341329
openSNPrs151341329
23andMers151341329
23andMe allrs151341329
SNP Nexus

SNPshotrs151341329
SNPdbers151341329
MSV3drs151341329
GWAS Ctlgrs151341329
Max Magnitude0
ClinVar
Risk rs151341329(C;C)
Alt rs151341329(C;C)
Reference rs151341329(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323966C>G
CLNSRC
CLNACC