common variants risk_factor_for OCD
Evidence from:
primary |
all sources
Evidence (5 sources)
Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder.
(2025)
PMID:38712091
primary
common variants explain only a modest amount of the phenotypic variation in OCD suggests that other types of genetic variation may also contribute
confidence: 0.92
Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder.
(2025)
PMID:38712091
primary
Common SNPs explained 6.7% of the variation in OCD risk in our meta-analysis
confidence: 0.95
The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum.
(2022)
PMID:34789012
cited
majority of inherited liability for OCD in Sweden traces to common genetic variation
confidence: 0.95
The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum.
(2022)
PMID:34789012
cited
substantial contribution of common variation to the heritability of OCD
confidence: 0.95
The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum.
(2022)
PMID:34789012
cited
SNP-based heritability estimate from common variation, 29%, suggests majority of inherited liability for OCD traces to common genetic variation.
confidence: 0.96