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rs3173419

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3173419(G;T)
Make rs3173419(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943342
GeneHLA-A
is asnp
is mentioned by
dbSNPrs3173419
ebirs3173419
HLIrs3173419
Exacrs3173419
Varsomers3173419
Maprs3173419
PheGenIrs3173419
hapmaprs3173419
1000 genomesrs3173419
hgdprs3173419
ensemblrs3173419
gopubmedrs3173419
geneviewrs3173419
scholarrs3173419
googlers3173419
pharmgkbrs3173419
gwascentralrs3173419
openSNPrs3173419
23andMers3173419
23andMe allrs3173419
SNP Nexus

SNPshotrs3173419
SNPdbers3173419
MSV3drs3173419
GWAS Ctlgrs3173419
GMAF0.4353
Max Magnitude0
ClinVar
Risk rs3173419(A,C,T;A,C,T)
Alt rs3173419(A,C,T;A,C,T)
Reference rs3173419(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911119G>A; NC_000006.11:g.29911119G>C; NC_000006.11:g.29911119G>T
CLNSRC
CLNACC


GET Evidence
HLA-A-D140H
aa_change Asp140His
aa_change_short D140H
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0625
summary