
SNP Report
| Name | rs1006737 dbSNP Ensembl |
|---|---|
| Location | Chrchr12:2345295(Forward) |
| Variant Alleles | G/A |
| Ancestral Allele | G |
| Annotation | intron_variant |
| Consequence to Transcript | intron_variant(ENST00000327702, ENST00000335762, ENST00000344100, ENST00000347598, ENST00000399591, ENST00000399595, ENST00000399597, ENST00000399601, ENST00000399603, ENST00000399606, ENST00000399617, ENST00000399621, ENST00000399629, ENST00000399634, ENST00000399637, ENST00000399638, ENST00000399641, ENST00000399644, ENST00000399649, ENST00000399655, ENST00000402845, ENST00000406454, ENST00000480911, LRG_334_t1, LRG_334_t2, LRG_334_t3, LRG_334_t4) |
| No. of Studies (Positive/Negative) | 2 (2/0)
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Note:
1. The different color of the nodes denotes the level of the nodes.
| Genetic/Epigenetic Locus | Protein and Other Molecule | Cell and Molecular Pathway | Neural System | Cognition and Behavior | Symptoms and Signs | Environment | MDD |
3. The network is generated using Cytoscape Web

