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rs1059467

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1059467(G;G)
Make rs1059467(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942966
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059467
ebirs1059467
HLIrs1059467
Exacrs1059467
Varsomers1059467
Maprs1059467
PheGenIrs1059467
hapmaprs1059467
1000 genomesrs1059467
hgdprs1059467
ensemblrs1059467
gopubmedrs1059467
geneviewrs1059467
scholarrs1059467
googlers1059467
pharmgkbrs1059467
gwascentralrs1059467
openSNPrs1059467
23andMers1059467
23andMe allrs1059467
SNP Nexus

SNPshotrs1059467
SNPdbers1059467
MSV3drs1059467
GWAS Ctlgrs1059467
Max Magnitude0
ClinVar
Risk rs1059467(A,C,G;A,C,G)
Alt rs1059467(A,C,G;A,C,G)
Reference rs1059467(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910743T>A; NC_000006.11:g.29910743T>C; NC_000006.11:g.29910743T>G
CLNSRC
CLNACC