SNP Report

Basic Information

Name	rs1167264 dbSNP Ensembl
Location	Chrchr1:49933045(Forward)
Variant Alleles	C/T
Ancestral Allele	T
Annotation	intron_variant; nc_transcript_variant
Consequence to Transcript	intron_variant(ENST00000371836, ENST00000371838, ENST00000371839, ENST00000457061) nc_transcript_variant(ENST00000457061)
No. of Studies (Positive/Negative)	1 (0/1)

Positive relationship between rs1167264 and MDD (count: 0)

Relationships between rs1167264 and other components at different levels (count: 0)

Negative relationships between rs1167264 and MDD (count: 1)

Reference	Research Type	Statistical Result	Relation Description
Shi, 2011	patients and normal controls	P-value <10-5	associated with MDD(P <10-5 in all subjects) associated with MDD(P <10-5 in all subjects)

Negative relationships between rs1167264 and other components at different levels (count: 0)

rs1167264 related genes (count: 2)

Approved Symbol	Approved Name	Type	No. of Studies (Positive/Negative)
AGBL4-IT1	AGBL4 intronic transcript 1 (non-protein coding)	SNP mapped	0(0/0)
AGBL4	ATP/GTP binding protein-like 4	SNP mapped	0(0/0)