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rs1059644

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1059644(A;A)
Make rs1059644(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944337
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059644
ebirs1059644
HLIrs1059644
Exacrs1059644
Varsomers1059644
Maprs1059644
PheGenIrs1059644
hapmaprs1059644
1000 genomesrs1059644
hgdprs1059644
ensemblrs1059644
gopubmedrs1059644
geneviewrs1059644
scholarrs1059644
googlers1059644
pharmgkbrs1059644
gwascentralrs1059644
openSNPrs1059644
23andMers1059644
23andMe allrs1059644
SNP Nexus

SNPshotrs1059644
SNPdbers1059644
MSV3drs1059644
GWAS Ctlgrs1059644
Max Magnitude0
ClinVar
Risk rs1059644(A;A)
Alt rs1059644(A;A)
Reference rs1059644(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912114C>A
CLNSRC
CLNACC