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rs151341132

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341132(A;A)
Make rs151341132(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356813
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341132
ebirs151341132
HLIrs151341132
Exacrs151341132
Varsomers151341132
Maprs151341132
PheGenIrs151341132
hapmaprs151341132
1000 genomesrs151341132
hgdprs151341132
ensemblrs151341132
gopubmedrs151341132
geneviewrs151341132
scholarrs151341132
googlers151341132
pharmgkbrs151341132
gwascentralrs151341132
openSNPrs151341132
23andMers151341132
23andMe allrs151341132
SNP Nexus

SNPshotrs151341132
SNPdbers151341132
MSV3drs151341132
GWAS Ctlgrs151341132
Merged fromRs151341133, Rs151341134
Max Magnitude0
ClinVar
Risk rs151341132(A,G,T;A,G,T)
Alt rs151341132(A,G,T;A,G,T)
Reference rs151341132(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324590G>A; NC_000006.11:g.31324590G>C; NC_000006.11:g.31324590G>T
CLNSRC
CLNACC