rs3750965
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3750965(A;A) |
| Make rs3750965(A;G) |
| Make rs3750965(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 69072692 |
| Gene | TPCN2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3750965 |
| dbSNP (classic) | rs3750965 |
| ClinGen | rs3750965 |
| ebi | rs3750965 |
| HLI | rs3750965 |
| Exac | rs3750965 |
| Gnomad | rs3750965 |
| Varsome | rs3750965 |
| LitVar | rs3750965 |
| Map | rs3750965 |
| PheGenI | rs3750965 |
| Biobank | rs3750965 |
| 1000 genomes | rs3750965 |
| hgdp | rs3750965 |
| ensembl | rs3750965 |
| geneview | rs3750965 |
| scholar | rs3750965 |
| rs3750965 | |
| pharmgkb | rs3750965 |
| gwascentral | rs3750965 |
| openSNP | rs3750965 |
| 23andMe | rs3750965 |
| SNPshot | rs3750965 |
| SNPdbe | rs3750965 |
| MSV3d | rs3750965 |
| GWAS Ctlg | rs3750965 |
| GMAF | 0.2548 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20585627 ]
|
| Trait | Hair color |
| Title | Web-based, participant-driven studies yield novel genetic associations for common traits |
| Risk Allele | |
| P-val | 3E-7 |
| Odds Ratio | None None |
[PMID 26918892] Genetic Variants of TPCN2 Associated with Type 2 Diabetes Risk in the Chinese Population.
