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rs1059488

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1059488(C;C)
Make rs1059488(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943321
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059488
ebirs1059488
HLIrs1059488
Exacrs1059488
Varsomers1059488
Maprs1059488
PheGenIrs1059488
hapmaprs1059488
1000 genomesrs1059488
hgdprs1059488
ensemblrs1059488
gopubmedrs1059488
geneviewrs1059488
scholarrs1059488
googlers1059488
pharmgkbrs1059488
gwascentralrs1059488
openSNPrs1059488
23andMers1059488
23andMe allrs1059488
SNP Nexus

SNPshotrs1059488
SNPdbers1059488
MSV3drs1059488
GWAS Ctlgrs1059488
GMAF0.03719
Max Magnitude0
ClinVar
Risk rs1059488(C,G;C,G)
Alt rs1059488(C,G;C,G)
Reference rs1059488(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911098T>C; NC_000006.11:g.29911098T>G
CLNSRC
CLNACC


GET Evidence
HLA-A-F133L
aa_change Phe133Leu
aa_change_short F133L
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.05447
summary