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rs151341269

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341269(A;C)
Make rs151341269(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356290
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341269
ebirs151341269
HLIrs151341269
Exacrs151341269
Varsomers151341269
Maprs151341269
PheGenIrs151341269
hapmaprs151341269
1000 genomesrs151341269
hgdprs151341269
ensemblrs151341269
gopubmedrs151341269
geneviewrs151341269
scholarrs151341269
googlers151341269
pharmgkbrs151341269
gwascentralrs151341269
openSNPrs151341269
23andMers151341269
23andMe allrs151341269
SNP Nexus

SNPshotrs151341269
SNPdbers151341269
MSV3drs151341269
GWAS Ctlgrs151341269
Max Magnitude0
ClinVar
Risk rs151341269(C,G;C,G)
Alt rs151341269(C,G;C,G)
Reference rs151341269(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324067T>C; NC_000006.11:g.31324067T>G
CLNSRC
CLNACC