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rs1059535

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1059535(C;T)
Make rs1059535(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943445
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059535
ebirs1059535
HLIrs1059535
Exacrs1059535
Varsomers1059535
Maprs1059535
PheGenIrs1059535
hapmaprs1059535
1000 genomesrs1059535
hgdprs1059535
ensemblrs1059535
gopubmedrs1059535
geneviewrs1059535
scholarrs1059535
googlers1059535
pharmgkbrs1059535
gwascentralrs1059535
openSNPrs1059535
23andMers1059535
23andMe allrs1059535
SNP Nexus

SNPshotrs1059535
SNPdbers1059535
MSV3drs1059535
GWAS Ctlgrs1059535
GMAF0.07071
Max Magnitude0
ClinVar
Risk rs1059535(T;T)
Alt rs1059535(T;T)
Reference rs1059535(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911222C; NC_000006.11:g.29911222C>T
CLNSRC
CLNACC


GET Evidence
HLA-A-A174V
aa_change Ala174Val
aa_change_short A174V
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.109675
summary