rs267603153
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs267603153(C;C) |
| Make rs267603153(C;T) |
| Make rs267603153(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 11 |
| Position | 69087152 |
| Gene | TPCN2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs267603153 |
| dbSNP (classic) | rs267603153 |
| ClinGen | rs267603153 |
| ebi | rs267603153 |
| HLI | rs267603153 |
| Exac | rs267603153 |
| Gnomad | rs267603153 |
| Varsome | rs267603153 |
| LitVar | rs267603153 |
| Map | rs267603153 |
| PheGenI | rs267603153 |
| Biobank | rs267603153 |
| 1000 genomes | rs267603153 |
| hgdp | rs267603153 |
| ensembl | rs267603153 |
| geneview | rs267603153 |
| scholar | rs267603153 |
| rs267603153 | |
| pharmgkb | rs267603153 |
| gwascentral | rs267603153 |
| openSNP | rs267603153 |
| 23andMe | rs267603153 |
| SNPshot | rs267603153 |
| SNPdbe | rs267603153 |
| MSV3d | rs267603153 |
| GWAS Ctlg | rs267603153 |
| Max Magnitude | 0 |
[PMID 26918892
] Genetic Variants of TPCN2 Associated with Type 2 Diabetes Risk in the Chinese Population.
