BCL2L1
From SNPedia
| is a | gene |
| is | mentioned by |
| Full name | BCL2-like 1 |
| EntrezGene | 598 |
| PheGenI | 598 |
| VariationViewer | 598 |
| ClinVar | BCL2L1 |
| GeneCards | BCL2L1 |
| dbSNP | 598 |
| Diseases | BCL2L1 |
| SADR | 598 |
| HugeNav | 598 |
| wikipedia | BCL2L1 |
| BCL2L1 | |
| gopubmed | BCL2L1 |
| EVS | BCL2L1 |
| HEFalMp | BCL2L1 |
| MyGene2 | BCL2L1 |
| 23andMe | BCL2L1 |
| UniProt | Q07817 |
| Ensembl | ENSG00000171552 |
| OMIM | 600039 |
| # SNPs | 2 |
| Max Magnitude | Chromosome position | Summary | |
|---|---|---|---|
| rs1484994 | 0 | 31,718,172 | |
| rs3208684 | 0 | 31,665,002 |
[PMID 25607358] Common genetic variants influence human subcortical brain structures.
