SNP Report

Basic Info

Name	rs11736084 dbSNP Ensembl
Location	chr4:8572220 - 8572220(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.157348
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000503448, ENST00000503981); non_coding_transcript_variant(ENST00000503448, ENST00000503981)
No. of Studies	2 (Positive: 0; Negative: 2; Trend: 0)
Source	Literature
Overlap with SZ?	YES
Overlap with MDD?	NO

SNP related studies (count: 2)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result Category
Yosifova, A.,2009	C/T		Allelic association: P-value = 0.29 Allelic association: P-value = 0.29	No significant association was observed No significant association was observed	Negative
Underwood, S. L., 2006	C/T		no P-value given in the text no P-value given in the text	No single-marker association was detected with any other SNP...... No single-marker association was detected with any other SNP, in the males or in the individuals with BPAD. More...	Negative

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
GPR78	G protein-coupled receptor 78	4p16.1	2(2/0/0)

SNPs in LD with rs11736084 (count: 0) View in gBrowse (chr4:8572220..8572220 )

Overlap with SZ from cross-disorder studies (count: 1)

Reference	Statistical Result	Description	Result Category
Underwood, S. L., 2006	no P-value given in the text	No single-marker association was detected.	Negative

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