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rs1059520

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1059520(A;A)
Make rs1059520(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943430
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059520
ebirs1059520
HLIrs1059520
Exacrs1059520
Varsomers1059520
Maprs1059520
PheGenIrs1059520
hapmaprs1059520
1000 genomesrs1059520
hgdprs1059520
ensemblrs1059520
gopubmedrs1059520
geneviewrs1059520
scholarrs1059520
googlers1059520
pharmgkbrs1059520
gwascentralrs1059520
openSNPrs1059520
23andMers1059520
23andMe allrs1059520
SNP Nexus

SNPshotrs1059520
SNPdbers1059520
MSV3drs1059520
GWAS Ctlgrs1059520
GMAF0.3255
Max Magnitude0
ClinVar
Risk rs1059520(A,C,T;A,C,T)
Alt rs1059520(A,C,T;A,C,T)
Reference rs1059520(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911207G>A; NC_000006.11:g.29911207G>C; NC_000006.11:g.29911207G>T
CLNSRC
CLNACC


GET Evidence
HLA-A-R169H
aa_change Arg169His
aa_change_short R169H
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.279333
summary