Have questions? Visit https://www.reddit.com/r/SNPedia

rs1059536

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1059536(A;G)
Make rs1059536(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943448
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059536
ebirs1059536
HLIrs1059536
Exacrs1059536
Varsomers1059536
Maprs1059536
PheGenIrs1059536
hapmaprs1059536
1000 genomesrs1059536
hgdprs1059536
ensemblrs1059536
gopubmedrs1059536
geneviewrs1059536
scholarrs1059536
googlers1059536
pharmgkbrs1059536
gwascentralrs1059536
openSNPrs1059536
23andMers1059536
23andMe allrs1059536
SNP Nexus

SNPshotrs1059536
SNPdbers1059536
MSV3drs1059536
GWAS Ctlgrs1059536
GMAF0.2277
Max Magnitude0
ClinVar
Risk rs1059536(G,T;G,T)
Alt rs1059536(G,T;G,T)
Reference rs1059536(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911225A>G; NC_000006.11:g.29911225A>T
CLNSRC
CLNACC


GET Evidence
HLA-A-H175R
aa_change His175Arg
aa_change_short H175R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.221585
summary