rs9494883
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs9494883(A;G) |
Make rs9494883(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 137850329 |
Gene | LOC100130476, LOC107986649 |
is a | snp |
is | mentioned by |
dbSNP | rs9494883 |
dbSNP (classic) | rs9494883 |
ClinGen | rs9494883 |
ebi | rs9494883 |
HLI | rs9494883 |
Exac | rs9494883 |
Gnomad | rs9494883 |
Varsome | rs9494883 |
LitVar | rs9494883 |
Map | rs9494883 |
PheGenI | rs9494883 |
Biobank | rs9494883 |
1000 genomes | rs9494883 |
hgdp | rs9494883 |
ensembl | rs9494883 |
geneview | rs9494883 |
scholar | rs9494883 |
rs9494883 | |
pharmgkb | rs9494883 |
gwascentral | rs9494883 |
openSNP | rs9494883 |
23andMe | rs9494883 |
SNPshot | rs9494883 |
SNPdbe | rs9494883 |
MSV3d | rs9494883 |
GWAS Ctlg | rs9494883 |
GMAF | 0.07759 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
association with lupus [PMID 19838195]
[PMID 19387456] Meta-analysis and imputation identifies a 109 kb risk haplotype spanning TNFAIP3 associated with lupus nephritis and hematologic manifestations.
[PMID 22488580] Brief report: candidate gene study in systemic sclerosis identifies a rare and functional variant of the TNFAIP3 locus as a risk factor for polyautoimmunity.