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rs74428022

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs74428022(C;T)
Make rs74428022(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355511
GeneHLA-B
is asnp
is mentioned by
dbSNPrs74428022
ebirs74428022
HLIrs74428022
Exacrs74428022
Varsomers74428022
Maprs74428022
PheGenIrs74428022
hapmaprs74428022
1000 genomesrs74428022
hgdprs74428022
ensemblrs74428022
gopubmedrs74428022
geneviewrs74428022
scholarrs74428022
googlers74428022
pharmgkbrs74428022
gwascentralrs74428022
openSNPrs74428022
23andMers74428022
23andMe allrs74428022
SNP Nexus

SNPshotrs74428022
SNPdbers74428022
MSV3drs74428022
GWAS Ctlgrs74428022
Max Magnitude0
ClinVar
Risk rs74428022(T;T)
Alt rs74428022(T;T)
Reference rs74428022(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323288G>A
CLNSRC
CLNACC