SNP Report

Basic Info

Name	rs2439286 dbSNP Ensembl
Location	chr8:32598664 - 32598664(1)
Variant Alleles	G/A/T
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.153954
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000287842, ENST00000356819, ENST00000405005, ENST00000518104, ENST00000519301, ENST00000520407, ENST00000521670, ENST00000523079, ENST00000523534, ENST00000631040)
No. of Studies	1 (Positive: 0; Negative: 1; Trend: 0)
Source	Literature
Overlap with SZ?	YES
Overlap with MDD?	NO

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result Category
Thomson, P. A., 2007			Individual P-value = 0.5884 for BP, Individual P-value = 0.5...... Individual P-value = 0.5884 for BP, Individual P-value = 0.5518 for SCZ and BP More...		Negative

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
NRG1	neuregulin 1	8p12	15(10/5/0)

SNPs in LD with rs2439286 (count: 3) View in gBrowse (chr8:32594380..32605183 )

The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r²<=0.8.

rs_ID	Functional Annotation	r²[population]
rs4602844	intron_variant	1.0[CEU]
rs2439284	intron_variant; upstream_gene_variant	0.828[CEU]
rs2439282	intron_variant; upstream_gene_variant	0.828[CEU]

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

Reference	Statistical Result	Description	Result Category
Thomson, P. A., 2007	Individual P-value = 0.6369 for SCZ , Individual P-value = 0.5518 for SCZ and BP		Negative

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