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rs1059542

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1059542(G;G)
Make rs1059542(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943479
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059542
ebirs1059542
HLIrs1059542
Exacrs1059542
Varsomers1059542
Maprs1059542
PheGenIrs1059542
hapmaprs1059542
1000 genomesrs1059542
hgdprs1059542
ensemblrs1059542
gopubmedrs1059542
geneviewrs1059542
scholarrs1059542
googlers1059542
pharmgkbrs1059542
gwascentralrs1059542
openSNPrs1059542
23andMers1059542
23andMe allrs1059542
SNP Nexus

SNPshotrs1059542
SNPdbers1059542
MSV3drs1059542
GWAS Ctlgrs1059542
GMAF0.1042
Max Magnitude0
ClinVar
Risk rs1059542(G;G)
Alt rs1059542(G;G)
Reference rs1059542(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911256T; NC_000006.11:g.29911256T>G
CLNSRC
CLNACC



GET Evidence
HLA-A-D185E
aa_change Asp185Glu
aa_change_short D185E
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.858937
summary