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rs1059418

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1059418(A;C)
Make rs1059418(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942785
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059418
ebirs1059418
HLIrs1059418
Exacrs1059418
Varsomers1059418
Maprs1059418
PheGenIrs1059418
hapmaprs1059418
1000 genomesrs1059418
hgdprs1059418
ensemblrs1059418
gopubmedrs1059418
geneviewrs1059418
scholarrs1059418
googlers1059418
pharmgkbrs1059418
gwascentralrs1059418
openSNPrs1059418
23andMers1059418
23andMe allrs1059418
SNP Nexus

SNPshotrs1059418
SNPdbers1059418
MSV3drs1059418
GWAS Ctlgrs1059418
GMAF0.1809
Max Magnitude0
ClinVar
Risk rs1059418(C,G,T;C,G,T)
Alt rs1059418(C,G,T;C,G,T)
Reference rs1059418(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910562A>C; NC_000006.11:g.29910562A>G; NC_000006.11:g.29910562A>T
CLNSRC
CLNACC