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rs151341098

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341098(C;T)
Make rs151341098(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356920
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341098
ebirs151341098
HLIrs151341098
Exacrs151341098
Varsomers151341098
Maprs151341098
PheGenIrs151341098
hapmaprs151341098
1000 genomesrs151341098
hgdprs151341098
ensemblrs151341098
gopubmedrs151341098
geneviewrs151341098
scholarrs151341098
googlers151341098
pharmgkbrs151341098
gwascentralrs151341098
openSNPrs151341098
23andMers151341098
23andMe allrs151341098
SNP Nexus

SNPshotrs151341098
SNPdbers151341098
MSV3drs151341098
GWAS Ctlgrs151341098
Max Magnitude0
ClinVar
Risk rs151341098(T;T)
Alt rs151341098(T;T)
Reference rs151341098(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324697G>A
CLNSRC
CLNACC