SNP Report

Basic Information

Name	rs12923267 dbSNP Ensembl
Location	Chrchr16:65538017(Forward)
Variant Alleles	C/T
Ancestral Allele	C
Annotation	intron_variant; nc_transcript_variant
Consequence to Transcript	intron_variant(ENST00000564041, ENST00000568492, ENST00000569736) nc_transcript_variant(ENST00000564041, ENST00000568492, ENST00000569736)
No. of Studies (Positive/Negative)	1 (0/1)

Positive relationship between rs12923267 and MDD (count: 0)

Relationships between rs12923267 and other components at different levels (count: 0)

Negative relationships between rs12923267 and MDD (count: 1)

Reference	Research Type	Statistical Result	Relation Description
Mahon PB, 2010	Patients and nomal controls	sample 1 p=0.003; sample 2 p=0.0048	Associated with MDD, sample 1 p=0.003; sample 2 p=0.0048 Associated with MDD, sample 1 p=0.003; sample 2 p=0.0048

Negative relationships between rs12923267 and other components at different levels (count: 0)

rs12923267 related genes (count: 0)