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rs151341361

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341361(C;T)
Make rs151341361(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355362
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341361
ebirs151341361
HLIrs151341361
Exacrs151341361
Varsomers151341361
Maprs151341361
PheGenIrs151341361
hapmaprs151341361
1000 genomesrs151341361
hgdprs151341361
ensemblrs151341361
gopubmedrs151341361
geneviewrs151341361
scholarrs151341361
googlers151341361
pharmgkbrs151341361
gwascentralrs151341361
openSNPrs151341361
23andMers151341361
23andMe allrs151341361
SNP Nexus

SNPshotrs151341361
SNPdbers151341361
MSV3drs151341361
GWAS Ctlgrs151341361
Max Magnitude0
ClinVar
Risk rs151341361(T;T)
Alt rs151341361(T;T)
Reference rs151341361(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323139G>A
CLNSRC
CLNACC