SNP Report

Basic Information

Name	rs17226852 dbSNP Ensembl
Location	Chrchr20:13973760(Forward)
Variant Alleles	T/C
Ancestral Allele	T
Annotation	intron_variant; nc_transcript_variant; upstream_gene_variant
Consequence to Transcript	intron_variant(ENST00000473203, ENST00000486903) nc_transcript_variant(ENST00000486903) upstream_gene_variant(ENST00000217246, ENST00000284951, ENST00000310348, ENST00000378072, ENST00000423870, ENST00000462552, ENST00000477147, ENST00000483997, ENST00000490428, ENST00000492055, ENST00000494602)
No. of Studies (Positive/Negative)	1 (0/1)

Positive relationship between rs17226852 and MDD (count: 0)

Relationships between rs17226852 and other components at different levels (count: 0)

Negative relationships between rs17226852 and MDD (count: 1)

Reference	Research Type	Statistical Result	Relation Description
Wray, 2010	patients and normal controls	P-value <10 -5	associated with MDD(P <10 -5) associated with MDD(P <10 -5)

Negative relationships between rs17226852 and other components at different levels (count: 0)

rs17226852 related genes (count: 2)

Approved Symbol	Approved Name	Type	No. of Studies (Positive/Negative)
MACROD2	MACRO domain containing 2	SNP mapped	0(0/0)
SEL1L2	sel-1 suppressor of lin-12-like 2 (C. elegans)	Literature-origin; SNP mapped	1(0/1)