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rs151341230

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341230(C;T)
Make rs151341230(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356387
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341230
ebirs151341230
HLIrs151341230
Exacrs151341230
Varsomers151341230
Maprs151341230
PheGenIrs151341230
hapmaprs151341230
1000 genomesrs151341230
hgdprs151341230
ensemblrs151341230
gopubmedrs151341230
geneviewrs151341230
scholarrs151341230
googlers151341230
pharmgkbrs151341230
gwascentralrs151341230
openSNPrs151341230
23andMers151341230
23andMe allrs151341230
SNP Nexus

SNPshotrs151341230
SNPdbers151341230
MSV3drs151341230
GWAS Ctlgrs151341230
Max Magnitude0
ClinVar
Risk rs151341230(T;T)
Alt rs151341230(T;T)
Reference rs151341230(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324164G>A
CLNSRC
CLNACC