SNP Report

Basic Information

Name	rs2253168 dbSNP Ensembl
Location	Chrchr14:69050465(Forward)
Variant Alleles	A/G
Ancestral Allele	G
Annotation	intron_variant; nc_transcript_variant
Consequence to Transcript	intron_variant(ENST00000390683, ENST00000478014, ENST00000487270, ENST00000487861, ENST00000488612, ENST00000553595, ENST00000554244, ENST00000556251) nc_transcript_variant(ENST00000478014, ENST00000553595, ENST00000554244)
No. of Studies (Positive/Negative)	1 (0/1)

Positive relationship between rs2253168 and MDD (count: 0)

Relationships between rs2253168 and other components at different levels (count: 0)

Negative relationships between rs2253168 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 rs2253168 and other components at different levels (count: 0)

rs2253168 related genes (count: 1)