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rs1059517

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1059517(A;C)
Make rs1059517(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943426
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059517
ebirs1059517
HLIrs1059517
Exacrs1059517
Varsomers1059517
Maprs1059517
PheGenIrs1059517
hapmaprs1059517
1000 genomesrs1059517
hgdprs1059517
ensemblrs1059517
gopubmedrs1059517
geneviewrs1059517
scholarrs1059517
googlers1059517
pharmgkbrs1059517
gwascentralrs1059517
openSNPrs1059517
23andMers1059517
23andMe allrs1059517
SNP Nexus

SNPshotrs1059517
SNPdbers1059517
MSV3drs1059517
GWAS Ctlgrs1059517
GMAF0.2925
Max Magnitude0
ClinVar
Risk rs1059517(C,G;C,G)
Alt rs1059517(C,G;C,G)
Reference rs1059517(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911203A>C; NC_000006.11:g.29911203A>G
CLNSRC
CLNACC


GET Evidence
HLA-A-K168Q
aa_change Lys168Gln
aa_change_short K168Q
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.326359
summary