rs176990
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs176990(G;G) |
Make rs176990(G;T) |
Make rs176990(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 139540945 |
Gene | LOC100507291, RBP1 |
is a | snp |
is | mentioned by |
dbSNP | rs176990 |
dbSNP (classic) | rs176990 |
ClinGen | rs176990 |
ebi | rs176990 |
HLI | rs176990 |
Exac | rs176990 |
Gnomad | rs176990 |
Varsome | rs176990 |
LitVar | rs176990 |
Map | rs176990 |
PheGenI | rs176990 |
Biobank | rs176990 |
1000 genomes | rs176990 |
hgdp | rs176990 |
ensembl | rs176990 |
geneview | rs176990 |
scholar | rs176990 |
rs176990 | |
pharmgkb | rs176990 |
gwascentral | rs176990 |
openSNP | rs176990 |
23andMe | rs176990 |
SNPshot | rs176990 |
SNPdbe | rs176990 |
MSV3d | rs176990 |
GWAS Ctlg | rs176990 |
GMAF | 0.3907 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 22171153] Association between a SLC23A2 gene variation, plasma vitamin C levels, and risk of glaucoma in a Mediterranean population