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rs1059563

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1059563(C;G)
Make rs1059563(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944151
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059563
ebirs1059563
HLIrs1059563
Exacrs1059563
Varsomers1059563
Maprs1059563
PheGenIrs1059563
hapmaprs1059563
1000 genomesrs1059563
hgdprs1059563
ensemblrs1059563
gopubmedrs1059563
geneviewrs1059563
scholarrs1059563
googlers1059563
pharmgkbrs1059563
gwascentralrs1059563
openSNPrs1059563
23andMers1059563
23andMe allrs1059563
SNP Nexus

SNPshotrs1059563
SNPdbers1059563
MSV3drs1059563
GWAS Ctlgrs1059563
Max Magnitude0
ClinVar
Risk rs1059563(A,G;A,G)
Alt rs1059563(A,G;A,G)
Reference rs1059563(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911928C>A; NC_000006.11:g.29911928C>G
CLNSRC
CLNACC


GET Evidence
HLA-A-PI217AV
aa_change ProIle217AlaVal
aa_change_short PI217AV
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.09375
summary