rs5029928
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs5029928(C;C) |
Make rs5029928(C;T) |
Make rs5029928(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 137868805 |
Gene | LOC100130476, TNFAIP3 |
is a | snp |
is | mentioned by |
dbSNP | rs5029928 |
dbSNP (classic) | rs5029928 |
ClinGen | rs5029928 |
ebi | rs5029928 |
HLI | rs5029928 |
Exac | rs5029928 |
Gnomad | rs5029928 |
Varsome | rs5029928 |
LitVar | rs5029928 |
Map | rs5029928 |
PheGenI | rs5029928 |
Biobank | rs5029928 |
1000 genomes | rs5029928 |
hgdp | rs5029928 |
ensembl | rs5029928 |
geneview | rs5029928 |
scholar | rs5029928 |
rs5029928 | |
pharmgkb | rs5029928 |
gwascentral | rs5029928 |
openSNP | rs5029928 |
23andMe | rs5029928 |
SNPshot | rs5029928 |
SNPdbe | rs5029928 |
MSV3d | rs5029928 |
GWAS Ctlg | rs5029928 |
GMAF | 0.1837 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23161053] TNFAIP3 gene polymorphisms confer risk for Behcet's disease in a Chinese Han population