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rs1059451

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1059451(A;A)
Make rs1059451(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942922
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059451
ebirs1059451
HLIrs1059451
Exacrs1059451
Varsomers1059451
Maprs1059451
PheGenIrs1059451
hapmaprs1059451
1000 genomesrs1059451
hgdprs1059451
ensemblrs1059451
gopubmedrs1059451
geneviewrs1059451
scholarrs1059451
googlers1059451
pharmgkbrs1059451
gwascentralrs1059451
openSNPrs1059451
23andMers1059451
23andMe allrs1059451
SNP Nexus

SNPshotrs1059451
SNPdbers1059451
MSV3drs1059451
GWAS Ctlgrs1059451
Max Magnitude0
ClinVar
Risk rs1059451(A;A)
Alt rs1059451(A;A)
Reference rs1059451(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910699G>A
CLNSRC
CLNACC