rs9909416
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9909416(C;C) |
Make rs9909416(C;T) |
Make rs9909416(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 35870979 |
Gene | LOC105371744 |
is a | snp |
is | mentioned by |
dbSNP | rs9909416 |
dbSNP (classic) | rs9909416 |
ClinGen | rs9909416 |
ebi | rs9909416 |
HLI | rs9909416 |
Exac | rs9909416 |
Gnomad | rs9909416 |
Varsome | rs9909416 |
LitVar | rs9909416 |
Map | rs9909416 |
PheGenI | rs9909416 |
Biobank | rs9909416 |
1000 genomes | rs9909416 |
hgdp | rs9909416 |
ensembl | rs9909416 |
geneview | rs9909416 |
scholar | rs9909416 |
rs9909416 | |
pharmgkb | rs9909416 |
gwascentral | rs9909416 |
openSNP | rs9909416 |
23andMe | rs9909416 |
SNPshot | rs9909416 |
SNPdbe | rs9909416 |
MSV3d | rs9909416 |
GWAS Ctlg | rs9909416 |
GMAF | 0.1997 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 18217191] Association of CC chemokine ligand 5 genotype with urinary albumin excretion in the non-diabetic Japanese general population: the Takahata study.