SNP Report

Basic Information

Name	rs493474 dbSNP Ensembl
Location	Chrchr1:199360977(Forward)
Variant Alleles	C/T
Ancestral Allele	C
Annotation	downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant
Consequence to Transcript	downstream_gene_variant(ENST00000430498) nc_transcript_variant(ENST00000452199) non_coding_exon_variant(ENST00000452199)
No. of Studies (Positive/Negative)	1 (0/1)

Positive relationship between rs493474 and MDD (count: 0)

Relationships between rs493474 and other components at different levels (count: 0)

Negative relationships between rs493474 and MDD (count: 1)

Reference	Research Type	Statistical Result	Relation Description
Shyn, 2011	patients and normal controls	P-value=0.0000413	best 25 results of the STARD GWAS( p=0.0000413) best 25 results of the STARD GWAS( p=0.0000413)

Negative relationships between rs493474 and other components at different levels (count: 0)

rs493474 related genes (count: 0)