SNP Report

Basic Info
Name rs4906236 dbSNP Ensembl
Location chr14:102610905 - 102610905(1)
Variant Alleles G/A
Ancestral Allele A
Minor Allele G
Minor Allele Frequence 0.324481
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000262241)
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
Gonzalez, S., 2014 Test for linkage: LOD=0.88, P-value=0.25; Test for associ...... Test for linkage: LOD=0.88, P-value=0.25; Test for association: LOD=0.48, P-value=0.139; Test for other linked variants: LOD=1.11, P-value=0.078 More... No significant associations were observed. No significant associations were observed. Negative

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
RCOR1 REST corepressor 1 14q32.33 1(0/1/0)

SNPs in LD with rs4906236 (count: 0) View in gBrowse (chr14:102610905..102610905 )

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

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