MK4MDD

SNP Report

Basic Information
Name rs10877887 dbSNP Ensembl
Location Chrchr12:62603400(Forward)
Variant Alleles T/C
Ancestral Allele T
Annotation regulatory_region_variant
Consequence to Transcript regulatory_region_variant(ENST00000362309, ENST00000550290, ENST00000408887, ENST00000623670, ENST00000619323, ENST00000393630)
No. of Studies (Positive/Negative) 1 (0/1) Help

Positive relationship between rs10877887 and MDD (count: 0)
Relationships between rs10877887 and other components at different levels (count: 0) Help
Negative relationships between rs10877887 and MDD (count: 1)
Reference Research Type Statistical Result Relation Description
Liang, 2015 Patients and nomal controls CC vs. TT: OR=1.73, 95% CI=1.04-2.86, P=0.03, and CC vs. TT/TC: OR=1.74, 95% CI=1.08¨C2.80, P=0.02 We found that the rs10877887 CC genotype was associated with...... We found that the rs10877887 CC genotype was associated with an increased risk of MDD (CC vs. TT: OR=1.73, 95% CI=1.04-2.86, P=0.03, and CC vs. TT/TC: OR=1.74, 95% CI=1.08¨C2.80, P=0.02, respectively). More...

Negative relationships between rs10877887 and other components at different levels (count: 0) Help
rs10877887 related genes (count: 0)