SNP Report

Basic Info

Name	rs362719 dbSNP Ensembl
Location	chr7:103545430 - 103545430(1)
Variant Alleles	C/A
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.416733
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000343529, ENST00000424685, ENST00000428762)
No. of Studies	1 (Positive: 1; Negative: 0; Trend: 0)
Source	Literature
Overlap with SZ?	NO
Overlap with MDD?	NO

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result Category
Goes, F. S., 2010		C	TDT test: P-value = 5.95E-4 OR=1.47[1.18-1.82] for all sampl...... TDT test: P-value = 5.95E-4 OR=1.47[1.18-1.82] for all samples, P-value = 8.95E-5 OR=1.79[1.33-2.44] for females, P-value = 0.49 OR=1.12[0.80-1.59] for males. More...	nominal significant and association remained significant aft...... nominal significant and association remained significant after empirical correction for testing of multiple markers; the strongest evidence of transmission distortion continued to be in affected females. More...	Positive

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
RELN	reelin	7q22	3(1/2/0)

SNPs in LD with rs362719 (count: 0) View in gBrowse (chr7:103545430..103545430 )

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)