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rs1059455

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1059455(C;G)
Make rs1059455(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942939
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059455
ebirs1059455
HLIrs1059455
Exacrs1059455
Varsomers1059455
Maprs1059455
PheGenIrs1059455
hapmaprs1059455
1000 genomesrs1059455
hgdprs1059455
ensemblrs1059455
gopubmedrs1059455
geneviewrs1059455
scholarrs1059455
googlers1059455
pharmgkbrs1059455
gwascentralrs1059455
openSNPrs1059455
23andMers1059455
23andMe allrs1059455
SNP Nexus

SNPshotrs1059455
SNPdbers1059455
MSV3drs1059455
GWAS Ctlgrs1059455
Max Magnitude0
ClinVar
Risk rs1059455(A,G;A,G)
Alt rs1059455(A,G;A,G)
Reference rs1059455(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910716C>A; NC_000006.11:g.29910716C>G
CLNSRC
CLNACC


GET Evidence
HLA-A-Q86Shift
aa_change Gln86Shift
aa_change_short Q86Shift
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency
summary