SNP Report

Basic Information

Name	rs4760933 dbSNP Ensembl
Location	Chrchr12:71143758(Forward)
Variant Alleles	A/G
Ancestral Allele	A
Annotation	intron_variant; nc_transcript_variant; NMD_transcript_variant
Consequence to Transcript	intron_variant(ENST00000283228, ENST00000342084, ENST00000378778, ENST00000440835, ENST00000548220, ENST00000549308, ENST00000550661, ENST00000551219) nc_transcript_variant(ENST00000548220) NMD_transcript_variant(ENST00000551219)
No. of Studies (Positive/Negative)	1 (0/1)

Positive relationship between rs4760933 and MDD (count: 0)

Relationships between rs4760933 and other components at different levels (count: 0)

Negative relationships between rs4760933 and MDD (count: 1)

Reference	Research Type	Statistical Result	Relation Description
Mahon PB, 2010	Patients and nomal controls	sample 1 p=0.000014; sample 2 p=0.53	Associated with MDD, sample 1 p=0.000014; sample 2 p=0.53 Associated with MDD, sample 1 p=0.000014; sample 2 p=0.53

Negative relationships between rs4760933 and other components at different levels (count: 0)

rs4760933 related genes (count: 1)