SNP Report

Basic Information

Name	rs6781822 dbSNP Ensembl
Location	Chrchr3:11675632(Forward)
Variant Alleles	T/C
Ancestral Allele	T
Annotation	intron_variant; NMD_transcript_variant; upstream_gene_variant
Consequence to Transcript	intron_variant(ENST00000273038, ENST00000404339, ENST00000417206, ENST00000417466, ENST00000418000, ENST00000419541, ENST00000426568, ENST00000430365, ENST00000445411) NMD_transcript_variant(ENST00000417466, ENST00000426568) upstream_gene_variant(ENST00000480288)
No. of Studies (Positive/Negative)	1 (0/1)

Positive relationship between rs6781822 and MDD (count: 0)

Relationships between rs6781822 and other components at different levels (count: 0)

Negative relationships between rs6781822 and MDD (count: 1)

Reference	Research Type	Statistical Result	Relation Description
Mahon PB, 2010	Patients and nomal controls	sample 1 p=0.0018; sample 2 p=0.0032	Associated with MDD, sample 1 p=0.0018; sample 2 p=0.0032 Associated with MDD, sample 1 p=0.0018; sample 2 p=0.0032

Negative relationships between rs6781822 and other components at different levels (count: 0)

rs6781822 related genes (count: 1)