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rs151341128

From SNPedia

Merged intors151341127
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341128(C;T)
Make rs151341128(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356817
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341128
ebirs151341128
HLIrs151341128
Exacrs151341128
Varsomers151341128
Maprs151341128
PheGenIrs151341128
hapmaprs151341128
1000 genomesrs151341128
hgdprs151341128
ensemblrs151341128
gopubmedrs151341128
geneviewrs151341128
scholarrs151341128
googlers151341128
pharmgkbrs151341128
gwascentralrs151341128
openSNPrs151341128
23andMers151341128
23andMe allrs151341128
SNP Nexus

SNPshotrs151341128
SNPdbers151341128
MSV3drs151341128
GWAS Ctlgrs151341128
StatusMerged into rs151341127
Max Magnitude0
ClinVar
Risk rs151341128(T;T)
Alt rs151341128(T;T)
Reference rs151341128(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324594G>A
CLNSRC
CLNACC