SNP Report

Basic Info

Name	rs169068 dbSNP Ensembl
Location	chr16:1079872 - 1079872(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.481829
Functional Annotation	missense_variant; upstream_gene_variant. Polyphen Annotation: benign(ENST00000293897) SIFT Annotation: tolerated(ENST00000293897)
Consequence to Transcript	missense_variant(ENST00000293897); upstream_gene_variant(ENST00000566499, ENST00000569832, ENST00000624643)
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/T		Allelic association: P-value = 0.15 Allelic association: P-value = 0.15	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)
SSTR5	somatostatin receptor 5	16p13.3	2(1/1/0)
SSTR5-AS1	SSTR5 antisense RNA 1	16p13.3	Mapped by Literature SNP

SNPs in LD with rs169068 (count: 0) View in gBrowse (chr16:1079872..1079872 )

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

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