rs117096873
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common genotype |
Make rs117096873(C;T) |
Make rs117096873(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 11293103 |
Gene | LOC105371082 |
is a | snp |
is | mentioned by |
dbSNP | rs117096873 |
dbSNP (classic) | rs117096873 |
ClinGen | rs117096873 |
ebi | rs117096873 |
HLI | rs117096873 |
Exac | rs117096873 |
Gnomad | rs117096873 |
Varsome | rs117096873 |
LitVar | rs117096873 |
Map | rs117096873 |
PheGenI | rs117096873 |
Biobank | rs117096873 |
1000 genomes | rs117096873 |
hgdp | rs117096873 |
ensembl | rs117096873 |
geneview | rs117096873 |
scholar | rs117096873 |
rs117096873 | |
pharmgkb | rs117096873 |
gwascentral | rs117096873 |
openSNP | rs117096873 |
23andMe | rs117096873 |
SNPshot | rs117096873 |
SNPdbe | rs117096873 |
MSV3d | rs117096873 |
GWAS Ctlg | rs117096873 |
GMAF | 0.006428 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 23568457] |
Trait | Bulimia nervosa |
Title | Genetic variants associated with disordered eating. |
Risk Allele | C |
P-val | 2E-6 |
Odds Ratio | .13 [0.076-0.182] unit decrease |