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

rs1059462

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1059462(C;C)
Make rs1059462(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942956
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059462
ebirs1059462
HLIrs1059462
Exacrs1059462
Varsomers1059462
Maprs1059462
PheGenIrs1059462
hapmaprs1059462
1000 genomesrs1059462
hgdprs1059462
ensemblrs1059462
gopubmedrs1059462
geneviewrs1059462
scholarrs1059462
googlers1059462
pharmgkbrs1059462
gwascentralrs1059462
openSNPrs1059462
23andMers1059462
23andMe allrs1059462
SNP Nexus

SNPshotrs1059462
SNPdbers1059462
MSV3drs1059462
GWAS Ctlgrs1059462
Max Magnitude0
ClinVar
Risk rs1059462(A,C;A,C)
Alt rs1059462(A,C;A,C)
Reference rs1059462(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910733G>A
CLNSRC
CLNACC