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rs3179982

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3179982(C;T)
Make rs3179982(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944556
GeneHLA-A
is asnp
is mentioned by
dbSNPrs3179982
ebirs3179982
HLIrs3179982
Exacrs3179982
Varsomers3179982
Maprs3179982
PheGenIrs3179982
hapmaprs3179982
1000 genomesrs3179982
hgdprs3179982
ensemblrs3179982
gopubmedrs3179982
geneviewrs3179982
scholarrs3179982
googlers3179982
pharmgkbrs3179982
gwascentralrs3179982
openSNPrs3179982
23andMers3179982
23andMe allrs3179982
SNP Nexus

SNPshotrs3179982
SNPdbers3179982
MSV3drs3179982
GWAS Ctlgrs3179982
GMAF0.466
Max Magnitude0
ClinVar
Risk rs3179982(T;T)
Alt rs3179982(T;T)
Reference rs3179982(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912333C>T
CLNSRC
CLNACC


GET Evidence
HLA-A-L318F
aa_change Leu318Phe
aa_change_short L318F
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.484973
summary