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rs1059449

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1059449(A;A)
Make rs1059449(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942921
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059449
ebirs1059449
HLIrs1059449
Exacrs1059449
Varsomers1059449
Maprs1059449
PheGenIrs1059449
hapmaprs1059449
1000 genomesrs1059449
hgdprs1059449
ensemblrs1059449
gopubmedrs1059449
geneviewrs1059449
scholarrs1059449
googlers1059449
pharmgkbrs1059449
gwascentralrs1059449
openSNPrs1059449
23andMers1059449
23andMe allrs1059449
SNP Nexus

SNPshotrs1059449
SNPdbers1059449
MSV3drs1059449
GWAS Ctlgrs1059449
GMAF0.1074
Max Magnitude0
ClinVar
Risk rs1059449(A;A)
Alt rs1059449(A;A)
Reference rs1059449(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910698G>A
CLNSRC
CLNACC


GET Evidence
HLA-A-G80R
aa_change Gly80Arg
aa_change_short G80R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0782964
summary