Have questions? Visit https://www.reddit.com/r/SNPedia

rs1059509

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1059509(A;A)
Make rs1059509(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943377
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059509
ebirs1059509
HLIrs1059509
Exacrs1059509
Varsomers1059509
Maprs1059509
PheGenIrs1059509
hapmaprs1059509
1000 genomesrs1059509
hgdprs1059509
ensemblrs1059509
gopubmedrs1059509
geneviewrs1059509
scholarrs1059509
googlers1059509
pharmgkbrs1059509
gwascentralrs1059509
openSNPrs1059509
23andMers1059509
23andMe allrs1059509
SNP Nexus

SNPshotrs1059509
SNPdbers1059509
MSV3drs1059509
GWAS Ctlgrs1059509
GMAF0.4715
Max Magnitude0
ClinVar
Risk rs1059509(A,G,T;A,G,T)
Alt rs1059509(A,G,T;A,G,T)
Reference rs1059509(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911154C>A; NC_000006.11:g.29911154C>G; NC_000006.11:g.29911154C>T
CLNSRC
CLNACC


GET Evidence
HLA-A-N151K
aa_change Asn151Lys
aa_change_short N151K
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.394113
summary