SNP Report

Name	rs40184 dbSNP Ensembl
Location	Chrchr5:1395077(Forward)
Variant Alleles	C/T
Ancestral Allele	T
Annotation	intron_variant
Consequence to Transcript	intron_variant(ENST00000270349, ENST00000453492, ENST00000512002)
No. of Studies (Positive/Negative)	2 (1/1)

Name in Literature	Related Components
	Level	Approved Name(Name in Literature)	Type	Reference	Research Type	Statistical Result	Relation Description	All
rs40184		Suicide(suicide attempt)	symptoms	Haeffel, 2008	nomal people		As hypothesized, one of the polymorphisms (rs40184) moderate...... As hypothesized, one of the polymorphisms (rs40184) moderated the effect of perceived maternal rejection on the onset of major depressive disorder, as well as on suicidal ideation More...

---

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

2. User can drag the nodes to rearrange the layout of the network. Click the node will enter the report page of the node. Right-click will show also the menus to link to the report page of the node and remove the node and related edges. Hover the node will show the level of the node and hover the edge will show the evidence/description of the edge.
3. The network is generated using Cytoscape Web

Reference	Research Type	Statistical Result	Relation Description
Pattarachotanant, 2010	patients and normal controls	chi(2) = 3.20, degrees of freedom = 1, P-value = 0.073, odds ratio = 0.53 [95% confidence interval = 0.28-1.01]	Although not significant, we observed more carriers of the C...... Although not significant, we observed more carriers of the C allele (CC+CT genotypes) in healthy controls than in patients with MDD (chi(2) = 3.20, degrees of freedom = 1, P = 0.073, odds ratio = 0.53 [95% confidence interval = 0.28-1.01]). More...

Approved Symbol	Approved Name	Type	No. of Studies (Positive/Negative)
SLC6A3	solute carrier family 6 (neurotransmitter transporter, dopamine), member 3	Literature-origin; SNP mapped; Protein mapped	3(2/1)