rs13077017
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13077017(C;C) |
Make rs13077017(C;T) |
Make rs13077017(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 58120049 |
Gene | FLNB |
is a | snp |
is | mentioned by |
dbSNP | rs13077017 |
dbSNP (classic) | rs13077017 |
ClinGen | rs13077017 |
ebi | rs13077017 |
HLI | rs13077017 |
Exac | rs13077017 |
Gnomad | rs13077017 |
Varsome | rs13077017 |
LitVar | rs13077017 |
Map | rs13077017 |
PheGenI | rs13077017 |
Biobank | rs13077017 |
1000 genomes | rs13077017 |
hgdp | rs13077017 |
ensembl | rs13077017 |
geneview | rs13077017 |
scholar | rs13077017 |
rs13077017 | |
pharmgkb | rs13077017 |
gwascentral | rs13077017 |
openSNP | rs13077017 |
23andMe | rs13077017 |
SNPshot | rs13077017 |
SNPdbe | rs13077017 |
MSV3d | rs13077017 |
GWAS Ctlg | rs13077017 |
GMAF | 0.1474 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23568457] |
Trait | Eating disorders (purging via substances) |
Title | Genetic variants associated with disordered eating. |
Risk Allele | C |
P-val | 1E-6 |
Odds Ratio | .07 [0.044-0.102] unit decrease |