SNP Report

Basic Info

Name	rs56690322 dbSNP Ensembl
Location	chrX:1615027 - 1615027(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.106629
Functional Annotation	5_prime_UTR_variant; upstream_gene_variant.
Consequence to Transcript	5_prime_UTR_variant(ENST00000381241); upstream_gene_variant(ENST00000381229, ENST00000381233)
No. of Studies	1 (Positive: 1; Negative: 0; 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
Etain, B.,2012		A	Allele association analysis: for French sample, P(value(Pc)=...... Allele association analysis: for French sample, P(value(Pc)=0.03(0.2), OR[95%CI]=1.48[1.03-2.13]; for German sample, P(value(Pc)=0.63(1), OR[95%CI]=1.08[0.79-1.46]; meta P(value=0.17, OR[95%CI]=1.23[0.98-1.55], Q=0.18 More...	Significant association was observed in BD. Significant association was observed in BD.	Positive

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
ASMT	acetylserotonin O-methyltransferase	Xp22.3 and Yp11.3	1(1/0/0)

SNPs in LD with rs56690322 (count: 0) View in gBrowse (chrX:1615027..1615027 )

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

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