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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
dbSNP (classic)rs1059536
ClinGenrs1059536
ebirs1059536
HLIrs1059536
Exacrs1059536
Gnomadrs1059536
Varsomers1059536
LitVarrs1059536
Maprs1059536
PheGenIrs1059536
Biobankrs1059536
1000 genomesrs1059536
hgdprs1059536
ensemblrs1059536
geneviewrs1059536
scholarrs1059536
googlers1059536
pharmgkbrs1059536
gwascentralrs1059536
openSNPrs1059536
23andMers1059536
SNPshotrs1059536
SNPdbers1059536
MSV3drs1059536
GWAS Ctlgrs1059536
GMAF0.2277
Max Magnitude0
ClinVar
Risk rs1059536(G;G) rs1059536(T;T)
Alt rs1059536(G;G) rs1059536(T;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