rs76765968
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs76765968(C;C) |
Make rs76765968(C;T) |
Make rs76765968(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 85934535 |
Gene | GRID1 |
is a | snp |
is | mentioned by |
dbSNP | rs76765968 |
dbSNP (classic) | rs76765968 |
ClinGen | rs76765968 |
ebi | rs76765968 |
HLI | rs76765968 |
Exac | rs76765968 |
Gnomad | rs76765968 |
Varsome | rs76765968 |
LitVar | rs76765968 |
Map | rs76765968 |
PheGenI | rs76765968 |
Biobank | rs76765968 |
1000 genomes | rs76765968 |
hgdp | rs76765968 |
ensembl | rs76765968 |
geneview | rs76765968 |
scholar | rs76765968 |
rs76765968 | |
pharmgkb | rs76765968 |
gwascentral | rs76765968 |
openSNP | rs76765968 |
23andMe | rs76765968 |
SNPshot | rs76765968 |
SNPdbe | rs76765968 |
MSV3d | rs76765968 |
GWAS Ctlg | rs76765968 |
GMAF | 0.07805 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 23568457] |
Trait | Anorexia nervosa |
Title | Genetic variants associated with disordered eating. |
Risk Allele | T |
P-val | 2E-6 |
Odds Ratio | .06 [0.037-0.091] unit decrease |