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rs151341328

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341328(C;C)
Make rs151341328(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356191
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341328
ebirs151341328
HLIrs151341328
Exacrs151341328
Varsomers151341328
Maprs151341328
PheGenIrs151341328
hapmaprs151341328
1000 genomesrs151341328
hgdprs151341328
ensemblrs151341328
gopubmedrs151341328
geneviewrs151341328
scholarrs151341328
googlers151341328
pharmgkbrs151341328
gwascentralrs151341328
openSNPrs151341328
23andMers151341328
23andMe allrs151341328
SNP Nexus

SNPshotrs151341328
SNPdbers151341328
MSV3drs151341328
GWAS Ctlgrs151341328
Max Magnitude0
ClinVar
Risk rs151341328(A,C;A,C)
Alt rs151341328(A,C;A,C)
Reference rs151341328(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323968C>G; NC_000006.11:g.31323968C>T
CLNSRC
CLNACC