SNP Report

Basic Information

Name	rs7596956 dbSNP Ensembl
Location	Chrchr2:220152359(Forward)
Variant Alleles	T/C
Ancestral Allele	C
Annotation	downstream_gene_variant
Consequence to Transcript	downstream_gene_variant(ENST00000295718, ENST00000336576, ENST00000392086, ENST00000392087, ENST00000409251, ENST00000423636, ENST00000425450, ENST00000439026, ENST00000442681, ENST00000443981, ENST00000460801, ENST00000462351, ENST00000463463, ENST00000470530, ENST00000472019, ENST00000473750, ENST00000476254, ENST00000477917, ENST00000480537, ENST00000487855, ENST00000497977, ENST00000537666, ENST00000539342)
No. of Studies (Positive/Negative)	1 (0/1)

Positive relationship between rs7596956 and MDD (count: 0)

Relationships between rs7596956 and other components at different levels (count: 0)

Negative relationships between rs7596956 and MDD (count: 1)

Reference	Research Type	Statistical Result	Relation Description
Mahon PB, 2010	Patients and nomal controls	sample 1 p=0.00087; sample 2 p=0.029	Associated with MDD, sample 1 p=0.00087; sample 2 p=0.029 Associated with MDD, sample 1 p=0.00087; sample 2 p=0.029

Negative relationships between rs7596956 and other components at different levels (count: 0)

rs7596956 related genes (count: 2)

Approved Symbol	Approved Name	Type	No. of Studies (Positive/Negative)
DNAJB2	DnaJ (Hsp40) homolog, subfamily B, member 2	SNP mapped	0(0/0)
PTPRN	protein tyrosine phosphatase, receptor type, N	SNP mapped	0(0/0)