
SNP Report
| Name | rs112439044 dbSNP Ensembl |
|---|---|
| Location | Chrchr1:41220077(Forward) |
| Variant Alleles | C/T |
| Ancestral Allele | C |
| Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
| Consequence to Transcript | downstream_gene_variant(ENST00000453631, ENST00000530965, ENST00000531464) intron_variant(ENST00000308733, ENST00000372651, ENST00000372652, ENST00000372653, ENST00000372654, ENST00000372669, ENST00000414185, ENST00000416859, ENST00000424419, ENST00000425457, ENST00000427410, ENST00000440226, ENST00000447388, ENST00000456393, ENST00000467203, ENST00000525290) nc_transcript_variant(ENST00000362104, ENST00000424419, ENST00000467203) non_coding_exon_variant(ENST00000362104) upstream_gene_variant(ENST00000385227, ENST00000525349) |
| No. of Studies (Positive/Negative) | 1 (1/0)
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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

