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rs1059452

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1059452(G;T)
Make rs1059452(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942923
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059452
ebirs1059452
HLIrs1059452
Exacrs1059452
Varsomers1059452
Maprs1059452
PheGenIrs1059452
hapmaprs1059452
1000 genomesrs1059452
hgdprs1059452
ensemblrs1059452
gopubmedrs1059452
geneviewrs1059452
scholarrs1059452
googlers1059452
pharmgkbrs1059452
gwascentralrs1059452
openSNPrs1059452
23andMers1059452
23andMe allrs1059452
SNP Nexus

SNPshotrs1059452
SNPdbers1059452
MSV3drs1059452
GWAS Ctlgrs1059452
GMAF0.2259
Max Magnitude0
ClinVar
Risk rs1059452(C,T;C,T)
Alt rs1059452(C,T;C,T)
Reference rs1059452(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910700G>C; NC_000006.11:g.29910700G>T
CLNSRC
CLNACC