SNP Report

Basic Info

Name	rs721629 dbSNP Ensembl
Location	chr8:18862672 - 18862672(1)
Variant Alleles	C/A
Ancestral Allele	C
Minor Allele	A
Minor Allele Frequence	0.3752
Functional Annotation	downstream_gene_variant; intron_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000623639); intron_variant(ENST00000327040, ENST00000440756, ENST00000523619)
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
Schirmbeck, F., 2007	G/T		no P-value given in the orignial article no P-value given in the orignial article	allele and haplotype frequencies did not differ between case...... allele and haplotype frequencies did not differ between cases and controls More...	Negative

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
PSD3	pleckstrin and Sec7 domain containing 3	8p21.3	Mapped by Literature SNP
SRR	serine racemase	17p13	1(0/1/0)

SNPs in LD with rs721629 (count: 0) View in gBrowse (chr8:18862672..18862672 )

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

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