rs469339
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs469339(A;A) |
Make rs469339(A;G) |
Make rs469339(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 94812833 |
Gene | MCTP1 |
is a | snp |
is | mentioned by |
dbSNP | rs469339 |
dbSNP (classic) | rs469339 |
ClinGen | rs469339 |
ebi | rs469339 |
HLI | rs469339 |
Exac | rs469339 |
Gnomad | rs469339 |
Varsome | rs469339 |
LitVar | rs469339 |
Map | rs469339 |
PheGenI | rs469339 |
Biobank | rs469339 |
1000 genomes | rs469339 |
hgdp | rs469339 |
ensembl | rs469339 |
geneview | rs469339 |
scholar | rs469339 |
rs469339 | |
pharmgkb | rs469339 |
gwascentral | rs469339 |
openSNP | rs469339 |
23andMe | rs469339 |
SNPshot | rs469339 |
SNPdbe | rs469339 |
MSV3d | rs469339 |
GWAS Ctlg | rs469339 |
GMAF | 0.08448 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23568457![]() |
Trait | Anorexia nervosa |
Title | Genetic variants associated with disordered eating. |
Risk Allele | A |
P-val | 3E-6 |
Odds Ratio | .14 [0.083-0.205] unit decrease |