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rs66585529

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs66585529(C;G)
Make rs66585529(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29945672
GeneHLA-A
is asnp
is mentioned by
dbSNPrs66585529
ebirs66585529
HLIrs66585529
Exacrs66585529
Varsomers66585529
Maprs66585529
PheGenIrs66585529
hapmaprs66585529
1000 genomesrs66585529
hgdprs66585529
ensemblrs66585529
gopubmedrs66585529
geneviewrs66585529
scholarrs66585529
googlers66585529
pharmgkbrs66585529
gwascentralrs66585529
openSNPrs66585529
23andMers66585529
23andMe allrs66585529
SNP Nexus

SNPshotrs66585529
SNPdbers66585529
MSV3drs66585529
GWAS Ctlgrs66585529
GMAF0.1556
Max Magnitude0
ClinVar
Risk rs66585529(G;G)
Alt rs66585529(G;G)
Reference rs66585529(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29913449C>G
CLNSRC
CLNACC