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rs1059686

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1059686(C;T)
Make rs1059686(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944370
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059686
ebirs1059686
HLIrs1059686
Exacrs1059686
Varsomers1059686
Maprs1059686
PheGenIrs1059686
hapmaprs1059686
1000 genomesrs1059686
hgdprs1059686
ensemblrs1059686
gopubmedrs1059686
geneviewrs1059686
scholarrs1059686
googlers1059686
pharmgkbrs1059686
gwascentralrs1059686
openSNPrs1059686
23andMers1059686
23andMe allrs1059686
SNP Nexus

SNPshotrs1059686
SNPdbers1059686
MSV3drs1059686
GWAS Ctlgrs1059686
GMAF0.3127
Max Magnitude0
ClinVar
Risk rs1059686(T;T)
Alt rs1059686(T;T)
Reference rs1059686(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912147C>T
CLNSRC
CLNACC