SNP Report

Basic Info
Name rs1585913 dbSNP Ensembl
Location chr10:44622528 - 44622528(1)
Variant Alleles G/A
Ancestral Allele A
Minor Allele A
Minor Allele Frequence 0.434904
No. of Studies 1 (Positive: 0; Negative: 0; Trend: 1)
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
Smith, E. N.,2011 A/G Genome-Wide Association: OR=0.79, P-value = 2.5E-06 Genome-Wide Association: OR=0.79, P-value = 2.5E-06 Suggestive association was found. Suggestive association was found. Trend

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
CXCL12 chemokine (C-X-C motif) ligand 12 10q11.1 1(0/0/1)

SNPs in LD with rs1585913 (count: 0) View in gBrowse (chr10:44622528..44622528 )

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

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