rs117124364
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common genotype |
Make rs117124364(C;T) |
Make rs117124364(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 32997453 |
is a | snp |
is | mentioned by |
dbSNP | rs117124364 |
dbSNP (classic) | rs117124364 |
ClinGen | rs117124364 |
ebi | rs117124364 |
HLI | rs117124364 |
Exac | rs117124364 |
Gnomad | rs117124364 |
Varsome | rs117124364 |
LitVar | rs117124364 |
Map | rs117124364 |
PheGenI | rs117124364 |
Biobank | rs117124364 |
1000 genomes | rs117124364 |
hgdp | rs117124364 |
ensembl | rs117124364 |
geneview | rs117124364 |
scholar | rs117124364 |
rs117124364 | |
pharmgkb | rs117124364 |
gwascentral | rs117124364 |
openSNP | rs117124364 |
23andMe | rs117124364 |
SNPshot | rs117124364 |
SNPdbe | rs117124364 |
MSV3d | rs117124364 |
GWAS Ctlg | rs117124364 |
GMAF | 0.005969 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 23568457] |
Trait | Bulimia nervosa |
Title | Genetic variants associated with disordered eating. |
Risk Allele | C |
P-val | 9E-6 |
Odds Ratio | .16 [0.089-0.231] unit decrease |