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rs1059564

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1059564(C;T)
Make rs1059564(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944153
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059564
ebirs1059564
HLIrs1059564
Exacrs1059564
Varsomers1059564
Maprs1059564
PheGenIrs1059564
hapmaprs1059564
1000 genomesrs1059564
hgdprs1059564
ensemblrs1059564
gopubmedrs1059564
geneviewrs1059564
scholarrs1059564
googlers1059564
pharmgkbrs1059564
gwascentralrs1059564
openSNPrs1059564
23andMers1059564
23andMe allrs1059564
SNP Nexus

SNPshotrs1059564
SNPdbers1059564
MSV3drs1059564
GWAS Ctlgrs1059564
Max Magnitude0
ClinVar
Risk rs1059564(T;T)
Alt rs1059564(T;T)
Reference rs1059564(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911930C>T
CLNSRC
CLNACC