SNP Report

Name	rs2073376 dbSNP Ensembl
Location	Chrchr21:47851753(Forward)
Variant Alleles	A/G
Ancestral Allele	G
Annotation	missense_variant; nc_transcript_variant; non_coding_exon_variant PolyPhen: benign(ENST00000359568) SIFT: tolerated(ENST00000359568)
Consequence to Transcript	missense_variant(ENST00000359568) nc_transcript_variant(ENST00000480896, ENST00000482575) non_coding_exon_variant(ENST00000480896, ENST00000482575)
No. of Studies (Positive/Negative)	1 (1/0)

Reference	Research Type	Statistical Result	Relation Description
Numata, 2009	patients and normal controls	P-value = 0.006	We found a significant allelic association between 3 SNPs (r...... We found a significant allelic association between 3 SNPs (rs3788265, rs2073376 and rs2073380) of the PCNT gene and MDD (p = 0.006, 0.005 and 0.021, respectively) 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)
PCNT	pericentrin	Literature-origin; SNP mapped	1(1/0)