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rs151341159

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341159(C;T)
Make rs151341159(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356799
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341159
ebirs151341159
HLIrs151341159
Exacrs151341159
Varsomers151341159
Maprs151341159
PheGenIrs151341159
hapmaprs151341159
1000 genomesrs151341159
hgdprs151341159
ensemblrs151341159
gopubmedrs151341159
geneviewrs151341159
scholarrs151341159
googlers151341159
pharmgkbrs151341159
gwascentralrs151341159
openSNPrs151341159
23andMers151341159
23andMe allrs151341159
SNP Nexus

SNPshotrs151341159
SNPdbers151341159
MSV3drs151341159
GWAS Ctlgrs151341159
Max Magnitude0
ClinVar
Risk rs151341159(G,T;G,T)
Alt rs151341159(G,T;G,T)
Reference rs151341159(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324576G>A; NC_000006.11:g.31324576G>C
CLNSRC
CLNACC