rs2069779
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs2069779(C;T) |
Make rs2069779(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 4 |
Position | 122452742 |
Gene | IL2 |
is a | snp |
is | mentioned by |
dbSNP | rs2069779 |
dbSNP (classic) | rs2069779 |
ClinGen | rs2069779 |
ebi | rs2069779 |
HLI | rs2069779 |
Exac | rs2069779 |
Gnomad | rs2069779 |
Varsome | rs2069779 |
LitVar | rs2069779 |
Map | rs2069779 |
PheGenI | rs2069779 |
Biobank | rs2069779 |
1000 genomes | rs2069779 |
hgdp | rs2069779 |
ensembl | rs2069779 |
geneview | rs2069779 |
scholar | rs2069779 |
rs2069779 | |
pharmgkb | rs2069779 |
gwascentral | rs2069779 |
openSNP | rs2069779 |
23andMe | rs2069779 |
SNPshot | rs2069779 |
SNPdbe | rs2069779 |
MSV3d | rs2069779 |
GWAS Ctlg | rs2069779 |
GMAF | 0.03673 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 21736829] Gene-PUFA interactions and obesity risk