SNP Report

Basic Information

Name	rs7127866 dbSNP Ensembl
Location	Chrchr11:82809600(Forward)
Variant Alleles	A/T
Ancestral Allele	T
Annotation	intron_variant; nc_transcript_variant; upstream_gene_variant
Consequence to Transcript	intron_variant(ENST00000527627) nc_transcript_variant(ENST00000527627) upstream_gene_variant(ENST00000533329)
No. of Studies (Positive/Negative)	1 (0/1)

Positive relationship between rs7127866 and MDD (count: 0)

Relationships between rs7127866 and other components at different levels (count: 0)

Negative relationships between rs7127866 and MDD (count: 1)

Reference	Research Type	Statistical Result	Relation Description
Shyn, 2011	patients and normal controls	P-value=0.000122	best 25 results of the STARD GWAS( p=0.000122) best 25 results of the STARD GWAS( p=0.000122)

Negative relationships between rs7127866 and other components at different levels (count: 0)

rs7127866 related genes (count: 0)