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rs1059516

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1059516(C;C)
Make rs1059516(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943421
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059516
ebirs1059516
HLIrs1059516
Exacrs1059516
Varsomers1059516
Maprs1059516
PheGenIrs1059516
hapmaprs1059516
1000 genomesrs1059516
hgdprs1059516
ensemblrs1059516
gopubmedrs1059516
geneviewrs1059516
scholarrs1059516
googlers1059516
pharmgkbrs1059516
gwascentralrs1059516
openSNPrs1059516
23andMers1059516
23andMe allrs1059516
SNP Nexus

SNPshotrs1059516
SNPdbers1059516
MSV3drs1059516
GWAS Ctlgrs1059516
Max Magnitude0
ClinVar
Risk rs1059516(C;C)
Alt rs1059516(C;C)
Reference rs1059516(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911198T>C
CLNSRC
CLNACC


GET Evidence
HLA-A-I166T
aa_change Ile166Thr
aa_change_short I166T
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.25874
summary