rs9658625
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common on affy axiom data |
Make rs9658625(A;G) |
Make rs9658625(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 53103618 |
Gene | SOAT2 |
is a | snp |
is | mentioned by |
dbSNP | rs9658625 |
dbSNP (classic) | rs9658625 |
ClinGen | rs9658625 |
ebi | rs9658625 |
HLI | rs9658625 |
Exac | rs9658625 |
Gnomad | rs9658625 |
Varsome | rs9658625 |
LitVar | rs9658625 |
Map | rs9658625 |
PheGenI | rs9658625 |
Biobank | rs9658625 |
1000 genomes | rs9658625 |
hgdp | rs9658625 |
ensembl | rs9658625 |
geneview | rs9658625 |
scholar | rs9658625 |
rs9658625 | |
pharmgkb | rs9658625 |
gwascentral | rs9658625 |
openSNP | rs9658625 |
23andMe | rs9658625 |
SNPshot | rs9658625 |
SNPdbe | rs9658625 |
MSV3d | rs9658625 |
GWAS Ctlg | rs9658625 |
GMAF | 0.09871 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19282863] Association of candidate gene polymorphisms with chronic kidney disease in Japanese individuals with hypertension