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rs3129018

From SNPedia

Merged intors3129017
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3129018(G;T)
Make rs3129018(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position29943484
GeneHLA-A
is asnp
is mentioned by
dbSNPrs3129018
ebirs3129018
HLIrs3129018
Exacrs3129018
Varsomers3129018
Maprs3129018
PheGenIrs3129018
hapmaprs3129018
1000 genomesrs3129018
hgdprs3129018
ensemblrs3129018
gopubmedrs3129018
geneviewrs3129018
scholarrs3129018
googlers3129018
pharmgkbrs3129018
gwascentralrs3129018
openSNPrs3129018
23andMers3129018
23andMe allrs3129018
SNP Nexus

SNPshotrs3129018
SNPdbers3129018
MSV3drs3129018
GWAS Ctlgrs3129018
StatusMerged into rs3129017
GMAF0.1653
Max Magnitude0
ClinVar
Risk rs3129018(A,C,T;A,C,T)
Alt rs3129018(A,C,T;A,C,T)
Reference rs3129018(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 1
HGVS NC_000006.11:g.29911261C>A; NC_000006.11:g.29911261C>G; NC_000006.11:g.29911261C>T
CLNSRC
CLNACC


GET Evidence
HLA-A-T187E
aa_change Thr187Glu
aa_change_short T187E
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0106383
summary