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rs1071816

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1071816(A;T)
Make rs1071816(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356759
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1071816
ebirs1071816
HLIrs1071816
Exacrs1071816
Varsomers1071816
Maprs1071816
PheGenIrs1071816
hapmaprs1071816
1000 genomesrs1071816
hgdprs1071816
ensemblrs1071816
gopubmedrs1071816
geneviewrs1071816
scholarrs1071816
googlers1071816
pharmgkbrs1071816
gwascentralrs1071816
openSNPrs1071816
23andMers1071816
23andMe allrs1071816
SNP Nexus

SNPshotrs1071816
SNPdbers1071816
MSV3drs1071816
GWAS Ctlgrs1071816
GMAF0.4564
Max Magnitude0
ClinVar
Risk rs1071816(C,G,T;C,G,T)
Alt rs1071816(C,G,T;C,G,T)
Reference rs1071816(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324536T>A; NC_000006.11:g.31324536T>C; NC_000006.11:g.31324536T>G
CLNSRC
CLNACC


[PMID 27157822] Genetic variants associated with antithyroid drug-induced agranulocytosis: a genome-wide association study in a European population.