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rs151341363

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341363(G;T)
Make rs151341363(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355342
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341363
ebirs151341363
HLIrs151341363
Exacrs151341363
Varsomers151341363
Maprs151341363
PheGenIrs151341363
hapmaprs151341363
1000 genomesrs151341363
hgdprs151341363
ensemblrs151341363
gopubmedrs151341363
geneviewrs151341363
scholarrs151341363
googlers151341363
pharmgkbrs151341363
gwascentralrs151341363
openSNPrs151341363
23andMers151341363
23andMe allrs151341363
SNP Nexus

SNPshotrs151341363
SNPdbers151341363
MSV3drs151341363
GWAS Ctlgrs151341363
Max Magnitude0
ClinVar
Risk rs151341363(T;T)
Alt rs151341363(T;T)
Reference rs151341363(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323119C>A
CLNSRC
CLNACC