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rs151341262

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341262(A;A)
Make rs151341262(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356293
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341262
ebirs151341262
HLIrs151341262
Exacrs151341262
Varsomers151341262
Maprs151341262
PheGenIrs151341262
hapmaprs151341262
1000 genomesrs151341262
hgdprs151341262
ensemblrs151341262
gopubmedrs151341262
geneviewrs151341262
scholarrs151341262
googlers151341262
pharmgkbrs151341262
gwascentralrs151341262
openSNPrs151341262
23andMers151341262
23andMe allrs151341262
SNP Nexus

SNPshotrs151341262
SNPdbers151341262
MSV3drs151341262
GWAS Ctlgrs151341262
Merged fromRs151341263, Rs151341264
Max Magnitude0
ClinVar
Risk rs151341262(A,G,T;A,G,T)
Alt rs151341262(A,G,T;A,G,T)
Reference rs151341262(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324070G>A; NC_000006.11:g.31324070G>C; NC_000006.11:g.31324070G>T
CLNSRC
CLNACC