SNP Report

Basic Info

Name	rs147825070 dbSNP Ensembl
Location	chr10:133088749 - 133088749(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.0071885
Functional Annotation	5_prime_UTR_variant; intron_variant; upstream_gene_variant.
Consequence to Transcript	5_prime_UTR_variant(ENST00000392607); intron_variant(ENST00000607359); upstream_gene_variant(ENST00000366099, ENST00000444433)
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
Ament, S. A., 2015			P-value=4.3e-5; q=8.9e-2 P-value=4.3e-5; q=8.9e-2	One of significant SNVs was a noncoding SNV in the 5' UTR of...... One of significant SNVs was a noncoding SNV in the 5' UTR of GPR123. More...	Positive

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
GPR123	adhesion G protein-coupled receptor A1	10q26	Mapped by Literature SNP

SNPs in LD with rs147825070 (count: 0) View in gBrowse (chr10:133088749..133088749 )

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

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