SNP Report

Basic Info

Name	rs1935952 dbSNP Ensembl
Location	chr6:108677702 - 108677702(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.481629
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000343882, ENST00000406360, ENST00000540898)
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
Magno, L. A.,2011	T/C		Chi-square tests: genotype: X²=6.59, P-value = 0....... Chi-square tests: genotype: X²=6.59, P-value = 0.0370; allele: X²=6.39, P-value = 0.0114 More...	Significant association was found . Significant association was found .	Positive

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
FOXO3	forkhead box O3	6q21	1(1/0/0)

SNPs in LD with rs1935952 (count: 0) View in gBrowse (chr6:108677702..108677702 )

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

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