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rs29028878

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs29028878(C;C)
Make rs29028878(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943950
GeneHLA-A
is asnp
is mentioned by
dbSNPrs29028878
dbSNP (classic)rs29028878
ClinGenrs29028878
ebirs29028878
HLIrs29028878
Exacrs29028878
Gnomadrs29028878
Varsomers29028878
LitVarrs29028878
Maprs29028878
PheGenIrs29028878
Biobankrs29028878
1000 genomesrs29028878
hgdprs29028878
ensemblrs29028878
geneviewrs29028878
scholarrs29028878
googlers29028878
pharmgkbrs29028878
gwascentralrs29028878
openSNPrs29028878
23andMers29028878
SNPshotrs29028878
SNPdbers29028878
MSV3drs29028878
GWAS Ctlgrs29028878
GMAF0.4206
Max Magnitude0
ClinVar
Risk rs29028878(C;C)
Alt rs29028878(C;C)
Reference Rs29028878(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911727T>C
CLNSRC
CLNACC