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rs1059632

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1059632(G;T)
Make rs1059632(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944310
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059632
ebirs1059632
HLIrs1059632
Exacrs1059632
Varsomers1059632
Maprs1059632
PheGenIrs1059632
hapmaprs1059632
1000 genomesrs1059632
hgdprs1059632
ensemblrs1059632
gopubmedrs1059632
geneviewrs1059632
scholarrs1059632
googlers1059632
pharmgkbrs1059632
gwascentralrs1059632
openSNPrs1059632
23andMers1059632
23andMe allrs1059632
SNP Nexus

SNPshotrs1059632
SNPdbers1059632
MSV3drs1059632
GWAS Ctlgrs1059632
Max Magnitude0
ClinVar
Risk rs1059632(A,T;A,T)
Alt rs1059632(A,T;A,T)
Reference rs1059632(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912087G>A; NC_000006.11:g.29912087G>T
CLNSRC
CLNACC