SNP Report

Name	rs3779250 dbSNP Ensembl
Location	Chrchr7:30694260(Forward)
Variant Alleles	C/T
Ancestral Allele	C
Annotation	intron_variant; NMD_transcript_variant
Consequence to Transcript	intron_variant(ENST00000341843, ENST00000348438, ENST00000452278, ENST00000471646, ENST00000506074) NMD_transcript_variant(ENST00000452278)
No. of Studies (Positive/Negative)	1 (1/0)

Reference	Research Type	Statistical Result	Relation Description
Ishitobi Y, 2012	patients and normal controls		The SNP rs110402 and rs242924 in the CRHR1 gene and the rs37...... The SNP rs110402 and rs242924 in the CRHR1 gene and the rs3779250 in the CRHR2 gene were associated with MDD More...

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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

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

Approved Symbol	Approved Name	Type	No. of Studies (Positive/Negative)
CRHR2	corticotropin releasing hormone receptor 2	Literature-origin; SNP mapped	1(0/1)