SNP Report

Basic Info

Name	rs3816360 dbSNP Ensembl
Location	chr11:13346203 - 13346203(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.496006
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000389707, ENST00000401424, ENST00000403290, ENST00000403510, ENST00000480685, ENST00000482049, ENST00000527998, ENST00000529050, ENST00000529388, ENST00000529825, ENST00000530357, ENST00000531665, ENST00000533520, ENST00000534544); non_coding_transcript_variant(ENST00000480685); upstream_gene_variant(ENST00000485918)
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
Dmitrzak-Weglarz, M. P., 2014	G/A		BPDII: P-value=0.0494, FDR=0.1888, OR=0.74, 95%CI=0.54-1.00. BPDII: P-value=0.0494, FDR=0.1888, OR=0.74, 95%CI=0.54-1.00.	Significant association was observed. Significant association was observed.	Positive

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
ARNTL	aryl hydrocarbon receptor nuclear translocator-like	11p15	7(5/2/0)

SNPs in LD with rs3816360 (count: 0) View in gBrowse (chr11:13346203..13346203 )

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

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