rs2288775
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2288775(A;A) |
Make rs2288775(A;G) |
Make rs2288775(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 58316132 |
Gene | NEDD4L |
is a | snp |
is | mentioned by |
dbSNP | rs2288775 |
dbSNP (classic) | rs2288775 |
ClinGen | rs2288775 |
ebi | rs2288775 |
HLI | rs2288775 |
Exac | rs2288775 |
Gnomad | rs2288775 |
Varsome | rs2288775 |
LitVar | rs2288775 |
Map | rs2288775 |
PheGenI | rs2288775 |
Biobank | rs2288775 |
1000 genomes | rs2288775 |
hgdp | rs2288775 |
ensembl | rs2288775 |
geneview | rs2288775 |
scholar | rs2288775 |
rs2288775 | |
pharmgkb | rs2288775 |
gwascentral | rs2288775 |
openSNP | rs2288775 |
23andMe | rs2288775 |
SNPshot | rs2288775 |
SNPdbe | rs2288775 |
MSV3d | rs2288775 |
GWAS Ctlg | rs2288775 |
GMAF | 0.2879 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20003179] Genetic variation of NEDD4L is associated with essential hypertension in female Kazakh general population: a case-control study
[PMID 24446284] Gender flip-flop association between genetic variations of NEDD4L and metabolic syndrome in the Kazakh general population