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rs1059846

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1059846(A;A)
Make rs1059846(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944549
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059846
ebirs1059846
HLIrs1059846
Exacrs1059846
Varsomers1059846
Maprs1059846
PheGenIrs1059846
hapmaprs1059846
1000 genomesrs1059846
hgdprs1059846
ensemblrs1059846
gopubmedrs1059846
geneviewrs1059846
scholarrs1059846
googlers1059846
pharmgkbrs1059846
gwascentralrs1059846
openSNPrs1059846
23andMers1059846
23andMe allrs1059846
SNP Nexus

SNPshotrs1059846
SNPdbers1059846
MSV3drs1059846
GWAS Ctlgrs1059846
GMAF0.1276
Max Magnitude0
ClinVar
Risk rs1059846(A;A)
Alt rs1059846(A;A)
Reference Rs1059846(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912326G>A
CLNSRC
CLNACC