rs180088
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs180088(A;A) |
Make rs180088(A;G) |
Make rs180088(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 17 |
Position | 69951455 |
is a | snp |
is | mentioned by |
dbSNP | rs180088 |
dbSNP (classic) | rs180088 |
ClinGen | rs180088 |
ebi | rs180088 |
HLI | rs180088 |
Exac | rs180088 |
Gnomad | rs180088 |
Varsome | rs180088 |
LitVar | rs180088 |
Map | rs180088 |
PheGenI | rs180088 |
Biobank | rs180088 |
1000 genomes | rs180088 |
hgdp | rs180088 |
ensembl | rs180088 |
geneview | rs180088 |
scholar | rs180088 |
rs180088 | |
pharmgkb | rs180088 |
gwascentral | rs180088 |
openSNP | rs180088 |
23andMe | rs180088 |
SNPshot | rs180088 |
SNPdbe | rs180088 |
MSV3d | rs180088 |
GWAS Ctlg | rs180088 |
GMAF | 0.2094 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19619703] Association of genetic variants with the metabolic syndrome in 20,806 white women: The women's health genome study