rs10494067
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs10494067(A;C) |
| Make rs10494067(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 107288236 |
| Gene | NTNG1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10494067 |
| dbSNP (classic) | rs10494067 |
| ClinGen | rs10494067 |
| ebi | rs10494067 |
| HLI | rs10494067 |
| Exac | rs10494067 |
| Gnomad | rs10494067 |
| Varsome | rs10494067 |
| LitVar | rs10494067 |
| Map | rs10494067 |
| PheGenI | rs10494067 |
| Biobank | rs10494067 |
| 1000 genomes | rs10494067 |
| hgdp | rs10494067 |
| ensembl | rs10494067 |
| geneview | rs10494067 |
| scholar | rs10494067 |
| rs10494067 | |
| pharmgkb | rs10494067 |
| gwascentral | rs10494067 |
| openSNP | rs10494067 |
| 23andMe | rs10494067 |
| SNPshot | rs10494067 |
| SNPdbe | rs10494067 |
| MSV3d | rs10494067 |
| GWAS Ctlg | rs10494067 |
| GMAF | 0.04821 |
| 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.
