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rs3180278

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs3180278(A;T)
Make rs3180278(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944568
GeneHLA-A
is asnp
is mentioned by
dbSNPrs3180278
ebirs3180278
HLIrs3180278
Exacrs3180278
Varsomers3180278
Maprs3180278
PheGenIrs3180278
hapmaprs3180278
1000 genomesrs3180278
hgdprs3180278
ensemblrs3180278
gopubmedrs3180278
geneviewrs3180278
scholarrs3180278
googlers3180278
pharmgkbrs3180278
gwascentralrs3180278
openSNPrs3180278
23andMers3180278
23andMe allrs3180278
SNP Nexus

SNPshotrs3180278
SNPdbers3180278
MSV3drs3180278
GWAS Ctlgrs3180278
GMAF0.1208
Max Magnitude0
ClinVar
Risk rs3180278(T;T)
Alt rs3180278(T;T)
Reference rs3180278(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912345A>T
CLNSRC
CLNACC


GET Evidence
HLA-A-I322V
aa_change Ile322Val
aa_change_short I322V
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0196078
summary