SNP Report

Basic Information

Name	rs4550218 dbSNP Ensembl
Location	Chrchr11:22863658(Forward)
Variant Alleles	C/G
Ancestral Allele	C
Annotation	downstream_gene_variant; intron_variant; nc_transcript_variant
Consequence to Transcript	downstream_gene_variant(ENST00000532798) intron_variant(ENST00000499625, ENST00000525963, ENST00000528701) nc_transcript_variant(ENST00000499625, ENST00000525963, ENST00000528701)
No. of Studies (Positive/Negative)	1 (0/1)

Positive relationship between rs4550218 and MDD (count: 0)

Relationships between rs4550218 and other components at different levels (count: 0)

Negative relationships between rs4550218 and MDD (count: 1)

Reference	Research Type	Statistical Result	Relation Description
Shyn, 2011	patients and normal controls	P-value=0.000071	best 25 results of the STARD GWAS( p=0.000071) best 25 results of the STARD GWAS( p=0.000071)

Negative relationships between rs4550218 and other components at different levels (count: 0)

rs4550218 related genes (count: 1)