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rs151341107

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341107(C;T)
Make rs151341107(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356881
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341107
ebirs151341107
HLIrs151341107
Exacrs151341107
Varsomers151341107
Maprs151341107
PheGenIrs151341107
hapmaprs151341107
1000 genomesrs151341107
hgdprs151341107
ensemblrs151341107
gopubmedrs151341107
geneviewrs151341107
scholarrs151341107
googlers151341107
pharmgkbrs151341107
gwascentralrs151341107
openSNPrs151341107
23andMers151341107
23andMe allrs151341107
SNP Nexus

SNPshotrs151341107
SNPdbers151341107
MSV3drs151341107
GWAS Ctlgrs151341107
Max Magnitude0
ClinVar
Risk rs151341107(T;T)
Alt rs151341107(T;T)
Reference rs151341107(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324658G>A
CLNSRC
CLNACC