SNP Report

Basic Information

Name	rs17299191 dbSNP Ensembl
Location	Chrchr16:55472083(Forward)
Variant Alleles	C/T
Ancestral Allele	C
Annotation	intron_variant; nc_transcript_variant
Consequence to Transcript	intron_variant(ENST00000565307, ENST00000569037, ENST00000570308) nc_transcript_variant(ENST00000565307, ENST00000569037)
No. of Studies (Positive/Negative)	1 (0/1)

Positive relationship between rs17299191 and MDD (count: 0)

Relationships between rs17299191 and other components at different levels (count: 0)

Negative relationships between rs17299191 and MDD (count: 1)

Reference	Research Type	Statistical Result	Relation Description
Mahon PB, 2010	Patients and nomal controls	sample 1 p=0.0045; sample 2 p=0.0073	Associated with MDD, sample 1 p=0.0045; sample 2 p=0.0073 Associated with MDD, sample 1 p=0.0045; sample 2 p=0.0073

Negative relationships between rs17299191 and other components at different levels (count: 0)

rs17299191 related genes (count: 1)