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rs1064588

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1064588(A;G)
Make rs1064588(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942940
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1064588
ebirs1064588
HLIrs1064588
Exacrs1064588
Varsomers1064588
Maprs1064588
PheGenIrs1064588
hapmaprs1064588
1000 genomesrs1064588
hgdprs1064588
ensemblrs1064588
gopubmedrs1064588
geneviewrs1064588
scholarrs1064588
googlers1064588
pharmgkbrs1064588
gwascentralrs1064588
openSNPrs1064588
23andMers1064588
23andMe allrs1064588
SNP Nexus

SNPshotrs1064588
SNPdbers1064588
MSV3drs1064588
GWAS Ctlgrs1064588
GMAF0.04775
Max Magnitude0
ClinVar
Risk rs1064588(C,G,T;C,G,T)
Alt rs1064588(C,G,T;C,G,T)
Reference rs1064588(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910717A>C; NC_000006.11:g.29910717A>G; NC_000006.11:g.29910717A>T
CLNSRC
CLNACC


GET Evidence
HLA-A-QE86LQ
aa_change GlnGlu86LeuGln
aa_change_short QE86LQ
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency
summary