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rs1143146

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1143146(C;G)
Make rs1143146(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942581
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1143146
ebirs1143146
HLIrs1143146
Exacrs1143146
Varsomers1143146
Maprs1143146
PheGenIrs1143146
hapmaprs1143146
1000 genomesrs1143146
hgdprs1143146
ensemblrs1143146
gopubmedrs1143146
geneviewrs1143146
scholarrs1143146
googlers1143146
pharmgkbrs1143146
gwascentralrs1143146
openSNPrs1143146
23andMers1143146
23andMe allrs1143146
SNP Nexus

SNPshotrs1143146
SNPdbers1143146
MSV3drs1143146
GWAS Ctlgrs1143146
GMAF0.478
Max Magnitude0
ClinVar
Risk rs1143146(G;G)
Alt rs1143146(G;G)
Reference rs1143146(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910358C>G
CLNSRC
CLNACC


GET Evidence
HLA-A-L10V
aa_change Leu10Val
aa_change_short L10V
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.4748
summary