rs114945094
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs114945094(A;A) |
Make rs114945094(A;G) |
Make rs114945094(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 12153806 |
is a | snp |
is | mentioned by |
dbSNP | rs114945094 |
dbSNP (classic) | rs114945094 |
ClinGen | rs114945094 |
ebi | rs114945094 |
HLI | rs114945094 |
Exac | rs114945094 |
Gnomad | rs114945094 |
Varsome | rs114945094 |
LitVar | rs114945094 |
Map | rs114945094 |
PheGenI | rs114945094 |
Biobank | rs114945094 |
1000 genomes | rs114945094 |
hgdp | rs114945094 |
ensembl | rs114945094 |
geneview | rs114945094 |
scholar | rs114945094 |
rs114945094 | |
pharmgkb | rs114945094 |
gwascentral | rs114945094 |
openSNP | rs114945094 |
23andMe | rs114945094 |
SNPshot | rs114945094 |
SNPdbe | rs114945094 |
MSV3d | rs114945094 |
GWAS Ctlg | rs114945094 |
GMAF | 0.2479 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 23568457] |
Trait | Anorexia nervosa |
Title | Genetic variants associated with disordered eating. |
Risk Allele | G |
P-val | 4E-6 |
Odds Ratio | .14 [0.078-0.192] unit decrease |