SNP Report

Name	rs11206244 dbSNP Ensembl
Location	Chrchr1:54375701(Forward)
Variant Alleles	C/T
Ancestral Allele	C
Annotation	3_prime_UTR_variant; downstream_gene_variant; NMD_transcript_variant
Consequence to Transcript	3_prime_UTR_variant(ENST00000322679, ENST00000361921, ENST00000525044, ENST00000527060, ENST00000528946, ENST00000530084) downstream_gene_variant(ENST00000388876, ENST00000524406, ENST00000525202, ENST00000529329, ENST00000529589, ENST00000532493, ENST00000534069) NMD_transcript_variant(ENST00000525044, ENST00000527060, ENST00000528946, ENST00000530084)
No. of Studies (Positive/Negative)	1 (1/0)

Reference	Research Type	Statistical Result	Relation Description
Philibert, 2011	patients and normal controls		We also found that rs11206244 genotype was associated with l...... We also found that rs11206244 genotype was associated with lifetime MD in White female subjects, in particular those from high-risk cohorts. 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)
DIO1	deiodinase, iodothyronine, type I	SNP mapped	0(0/0)