rs2383378
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2383378(A;A) |
Make rs2383378(A;C) |
Make rs2383378(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 32813264 |
Gene | AKAP6 |
is a | snp |
is | mentioned by |
dbSNP | rs2383378 |
dbSNP (classic) | rs2383378 |
ClinGen | rs2383378 |
ebi | rs2383378 |
HLI | rs2383378 |
Exac | rs2383378 |
Gnomad | rs2383378 |
Varsome | rs2383378 |
LitVar | rs2383378 |
Map | rs2383378 |
PheGenI | rs2383378 |
Biobank | rs2383378 |
1000 genomes | rs2383378 |
hgdp | rs2383378 |
ensembl | rs2383378 |
geneview | rs2383378 |
scholar | rs2383378 |
rs2383378 | |
pharmgkb | rs2383378 |
gwascentral | rs2383378 |
openSNP | rs2383378 |
23andMe | rs2383378 |
SNPshot | rs2383378 |
SNPdbe | rs2383378 |
MSV3d | rs2383378 |
GWAS Ctlg | rs2383378 |
GMAF | 0.2208 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21079607] |
Trait | |
Title | A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa |
Risk Allele | |
P-val | 0.000006 |
Odds Ratio | None None |
[PMID 23568457] Genetic variants associated with disordered eating.
[PMID 21079607] A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.