SNP Report

Basic Info

Name	rs3783006 dbSNP Ensembl
Location	chr13:98458955 - 98458955(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.357827
Functional Annotation	downstream_gene_variant; intron_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000319562); intron_variant(ENST00000376547, ENST00000376554, ENST00000397517, ENST00000418038, ENST00000444574, ENST00000539966)
No. of Studies	1 (Positive: 0; Negative: 1; 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
Yosifova, A.,2009	C/G		Allelic association: P-value = 0.35 Allelic association: P-value = 0.35	No significant association was observed No significant association was observed	Negative

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
FARP1	FERM, RhoGEF (ARHGEF) and pleckstrin domain protein 1 (chondrocyte-derived)	13q32.2	1(1/0/0)
STK24	serine/threonine kinase 24	13q31.2-q32.3	2(1/1/0)

SNPs in LD with rs3783006 (count: 0) View in gBrowse (chr13:98458955..98458955 )

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

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