SNP Report

Basic Info

Name	rs6644635 dbSNP Ensembl
Location	chrX:1615101 - 1615101(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.294529
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: 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
Etain, B.,2012		T	Allele association analysis: for French sample, P(value(Pc)=...... Allele association analysis: for French sample, P(value(Pc)=0.64(1), OR[95%CI]=1.06[0.84-1.33]; for German sample, P(value(Pc)=0.67(1), OR[95%CI]=0.96[0.80-1.15]; meta P(value=0.96, OR[95%CI]=1[0.87-1.15], Q=0.53 More...	No significant association was observed in BD. No significant association was observed in BD.	Negative

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 rs6644635 (count: 0) View in gBrowse (chrX:1615101..1615101 )

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

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