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rs1059426

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1059426(C;T)
Make rs1059426(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942806
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059426
ebirs1059426
HLIrs1059426
Exacrs1059426
Varsomers1059426
Maprs1059426
PheGenIrs1059426
hapmaprs1059426
1000 genomesrs1059426
hgdprs1059426
ensemblrs1059426
gopubmedrs1059426
geneviewrs1059426
scholarrs1059426
googlers1059426
pharmgkbrs1059426
gwascentralrs1059426
openSNPrs1059426
23andMers1059426
23andMe allrs1059426
SNP Nexus

SNPshotrs1059426
SNPdbers1059426
MSV3drs1059426
GWAS Ctlgrs1059426
GMAF0.1097
Max Magnitude0
ClinVar
Risk rs1059426(T;T)
Alt rs1059426(T;T)
Reference rs1059426(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910583C>T
CLNSRC
CLNACC