SNP Report

Basic Info

Name	rs7333687 dbSNP Ensembl
Location	chr13:98838305 - 98838305(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.458067
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000439367); intron_variant(ENST00000339416, ENST00000340449, ENST00000376460, ENST00000442173, ENST00000448493, ENST00000449796, ENST00000450257, ENST00000630992); NMD_transcript_variant(ENST00000339416, ENST00000630992)
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
Detera-Wadleigh, S. D., 2007			FBAT-e P-value = 0.352 in NIMH1-2, FBAT-e P-value = 0.8518 i...... FBAT-e P-value = 0.352 in NIMH1-2, FBAT-e P-value = 0.8518 in NIMH3, FBAT-e P-value = 0.3033 in NIMH4 More...	no significant over-transmission of any alleles was detected no significant over-transmission of any alleles was detected	Negative

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
DOCK9	dedicator of cytokinesis 9	13q32.3	1(1/0/0)
DOCK9-AS1	DOCK9 antisense RNA 1	13q32.3	Mapped by Literature SNP

SNPs in LD with rs7333687 (count: 0) View in gBrowse (chr13:98838305..98838305 )

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

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