SNP Report

Basic Info

Name	rs7331595 dbSNP Ensembl
Location	chr13:98945478 - 98945478(1)
Variant Alleles	C/A
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.465056
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000417594); intron_variant(ENST00000339416, ENST00000376460, ENST00000427887, ENST00000442173, ENST00000448493, ENST00000627024, 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 = 0.435 in NIMH1-2 FBAT-e P-value = 0.435 in NIMH1-2	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)
RPL7L1P12	ribosomal protein L7-like 1 pseudogene 12	13q32.3	Mapped by Literature SNP
DOCK9	dedicator of cytokinesis 9	13q32.3	1(1/0/0)

SNPs in LD with rs7331595 (count: 0) View in gBrowse (chr13:98945478..98945478 )

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

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