SNP Report

Basic Information

Name	rs9311395 dbSNP Ensembl
Location	Chrchr3:4741821(Forward)
Variant Alleles	A/G
Ancestral Allele	G
Annotation	intron_variant
Consequence to Transcript	intron_variant(ENST00000302640, ENST00000354582, ENST00000357086, ENST00000423119, ENST00000443694, ENST00000456211, ENST00000544951)
No. of Studies (Positive/Negative)	1 (0/1)

Positive relationship between rs9311395 and MDD (count: 0)

Relationships between rs9311395 and other components at different levels (count: 0)

Negative relationships between rs9311395 and MDD (count: 1)

Reference	Research Type	Statistical Result	Relation Description
Mahon PB, 2010	Patients and nomal controls	sample 1 p=0.0015; sample 2 p=0.022	Associated with MDD, sample 1 p=0.0015; sample 2 p=0.022 Associated with MDD, sample 1 p=0.0015; sample 2 p=0.022

Negative relationships between rs9311395 and other components at different levels (count: 0)

rs9311395 related genes (count: 1)