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rs1059438

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1059438(A;T)
Make rs1059438(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942846
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059438
ebirs1059438
HLIrs1059438
Exacrs1059438
Varsomers1059438
Maprs1059438
PheGenIrs1059438
hapmaprs1059438
1000 genomesrs1059438
hgdprs1059438
ensemblrs1059438
gopubmedrs1059438
geneviewrs1059438
scholarrs1059438
googlers1059438
pharmgkbrs1059438
gwascentralrs1059438
openSNPrs1059438
23andMers1059438
23andMe allrs1059438
SNP Nexus

SNPshotrs1059438
SNPdbers1059438
MSV3drs1059438
GWAS Ctlgrs1059438
GMAF0.002755
Max Magnitude0
ClinVar
Risk rs1059438(C,G,T;C,G,T)
Alt rs1059438(C,G,T;C,G,T)
Reference rs1059438(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910623A>C; NC_000006.11:g.29910623A>G; NC_000006.11:g.29910623A>T
CLNSRC
CLNACC