rs975121
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs975121(A;A) |
| Make rs975121(A;G) |
| Make rs975121(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 192179429 |
| Gene | FGF12 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs975121 |
| dbSNP (classic) | rs975121 |
| ClinGen | rs975121 |
| ebi | rs975121 |
| HLI | rs975121 |
| Exac | rs975121 |
| Gnomad | rs975121 |
| Varsome | rs975121 |
| LitVar | rs975121 |
| Map | rs975121 |
| PheGenI | rs975121 |
| Biobank | rs975121 |
| 1000 genomes | rs975121 |
| hgdp | rs975121 |
| ensembl | rs975121 |
| geneview | rs975121 |
| scholar | rs975121 |
| rs975121 | |
| pharmgkb | rs975121 |
| gwascentral | rs975121 |
| openSNP | rs975121 |
| 23andMe | rs975121 |
| SNPshot | rs975121 |
| SNPdbe | rs975121 |
| MSV3d | rs975121 |
| GWAS Ctlg | rs975121 |
| GMAF | 0.2658 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21139019 ]
|
| Trait | |
| Title | A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum |
| Risk Allele | |
| P-val | 0.000007 |
| Odds Ratio | 2.1700 [1.55-3.03] |
