SNP Report

Basic Information

Name	rs2116624 dbSNP Ensembl
Location	Chrchr7:13404664(Forward)
Variant Alleles	A/G
Ancestral Allele	A
Annotation	intron_variant; nc_transcript_variant; non_coding_exon_variant
Consequence to Transcript	intron_variant(ENST00000411542) nc_transcript_variant(ENST00000411542, ENST00000456809) non_coding_exon_variant(ENST00000456809)
No. of Studies (Positive/Negative)	1 (0/1)

Positive relationship between rs2116624 and MDD (count: 0)

Relationships between rs2116624 and other components at different levels (count: 0)

Negative relationships between rs2116624 and MDD (count: 1)

Reference	Research Type	Statistical Result	Relation Description
Shyn, 2011	patients and normal controls	P-value=0.000118	best 25 results of the STARD GWAS( p=0.000118) best 25 results of the STARD GWAS( p=0.000118)

Negative relationships between rs2116624 and other components at different levels (count: 0)

rs2116624 related genes (count: 0)