SNP Report

Basic Information

Name	rs7797729 dbSNP Ensembl
Location	Chrchr7:129310092(Forward)
Variant Alleles	T/C
Ancestral Allele	T
Annotation	intron_variant
Consequence to Transcript	intron_variant(ENST00000223190, ENST00000311967, ENST00000353868, ENST00000393230, ENST00000393231, ENST00000393232, ENST00000454688, ENST00000539636)
No. of Studies (Positive/Negative)	1 (0/1)

Positive relationship between rs7797729 and MDD (count: 0)

Relationships between rs7797729 and other components at different levels (count: 0)

Negative relationships between rs7797729 and MDD (count: 1)

Reference	Research Type	Statistical Result	Relation Description
Wray, 2010	patients and normal controls	P-value <10 -5	associated with MDD(P <10 -5) associated with MDD(P <10 -5)

Negative relationships between rs7797729 and other components at different levels (count: 0)

rs7797729 related genes (count: 1)