SNP Report

Basic Info
Name rs748856 dbSNP Ensembl
Location chr8:122802586 - 122802586(1)
Variant Alleles C/T
Ancestral Allele C
Minor Allele T
Minor Allele Frequence 0.497005
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000314393)
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
Gonzalez, S., 2014 Test for linkage: LOD=2.09, P-value=0.022; Test for assoc...... Test for linkage: LOD=2.09, P-value=0.022; Test for association: LOD=1.65, P-value=0.006; Test for other linked variants: LOD=2.21, P-value=0.006 More... It showed little evidence for association with BD. It showed little evidence for association with BD. Trend

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
ZHX2 zinc fingers and homeoboxes 2 8q24.13 1(0/0/1)

SNPs in LD with rs748856 (count: 0) View in gBrowse (chr8:122802586..122802586 )

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

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