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rs151341287

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341287(C;C)
Make rs151341287(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356275
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341287
ebirs151341287
HLIrs151341287
Exacrs151341287
Varsomers151341287
Maprs151341287
PheGenIrs151341287
hapmaprs151341287
1000 genomesrs151341287
hgdprs151341287
ensemblrs151341287
gopubmedrs151341287
geneviewrs151341287
scholarrs151341287
googlers151341287
pharmgkbrs151341287
gwascentralrs151341287
openSNPrs151341287
23andMers151341287
23andMe allrs151341287
SNP Nexus

SNPshotrs151341287
SNPdbers151341287
MSV3drs151341287
GWAS Ctlgrs151341287
Max Magnitude0
ClinVar
Risk rs151341287(C;C)
Alt rs151341287(C;C)
Reference rs151341287(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324052A>G
CLNSRC
CLNACC