PLXNB3
From SNPedia
| is a | gene |
| is | mentioned by |
| EntrezGene | 5365 |
| PheGenI | 5365 |
| VariationViewer | 5365 |
| ClinVar | PLXNB3 |
| GeneCards | PLXNB3 |
| dbSNP | 5365 |
| Diseases | PLXNB3 |
| SADR | 5365 |
| HugeNav | 5365 |
| wikipedia | PLXNB3 |
| PLXNB3 | |
| gopubmed | PLXNB3 |
| EVS | PLXNB3 |
| HEFalMp | PLXNB3 |
| MyGene2 | PLXNB3 |
| 23andMe | PLXNB3 |
| # SNPs | 2 |
| Max Magnitude | Chromosome position | Summary | |
|---|---|---|---|
| rs2266879 | 0 | 153,770,343 | |
| rs6643791 | 0 | 153,774,047 |
[PMID 17033634] - a human specific 'haplotype A' in PLXNB3, predicted by V598I (rs2266879), E1156D (rs6643791), and V1596E, associated with higher scores of vocabulary (WST) and increased white matter volume. the effect was significant for all groups tested (303 healthy volunteers, 42 male schizophrenics).
