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common variants cohort

Aliases
543 common SNPs (MAF ≥ 0.05), Common variants, Illumina markers, MAF ≥1% variants, SNP, SNPs, all common SNPs, common SNP, common SNPs, common SNPs of small effect, common alleles, common disease associated variant, common gene variant, common genetic variants, common genetic variation, common loci, common single nucleotide polymorphism, common single nucleotide polymorphisms, common variant, common variant association, common variants, common variants (MAF >5%), common variation, common variations, common, genome-wide SNPs, common-disease/common-variant, genome-wide SNPs, high-frequency variant, highly common variants, individual common variants, single nucleotide polymorphisms
Evidence from: primary | all sources

Related entities (121)

SubjectRelationObjectp-valueEvidence
African American associated_with common variants — 1
candidate genes associated_with common variants — 1
common variants risk_factor_for addiction — 1
common variants associated_with ADHD 0 1
common variants risk_factor_for ADHD — 2
common variants associated_with African American — 2
common variants associated_with African-Americans — 1
common variants associated_with age of onset — 1
common variants associated_with age-related macular degeneration — 2
common variants risk_factor_for alcohol — 2
common variants associated_with alcohol — 1
common variants risk_factor_for alcohol dependence 0.0047 2
common variants associated_with alcohol dependence — 2
common variants associated_with Alcohol Initiation — 1
common variants risk_factor_for Alcohol Use — 1
common variants associated_with Alcohol Use — 1
common variants associated_with Alcohol Use Disorder — 1
common variants associated_with alpha peak frequency — 2
common variants associated_with alpha power — 2
common variants risk_factor_for Alzheimer's disease — 1
common variants associated_with Alzheimer's disease — 2
common variants associated_with ancestry groups — 1
common variants risk_factor_for anorexia nervosa — 1
common variants associated_with anorexia nervosa — 1
common variants associated_with anxiety — 1
common variants associated_with AP — 1
common variants risk_factor_for AP — 1
common variants associated_with attention deficit hyperactivity disorder — 2
common variants risk_factor_for autism — 1
common variants associated_with autism — 1
common variants risk_factor_for autism spectrum disorder — 1
common variants associated_with autism spectrum disorders — 1
common variants associated_with behavior — 1
common variants associated_with beta power — 2
common variants associated_with bipolar disorder — 4
common variants risk_factor_for bipolar disorder — 2
common variants associated_with BMI — 1
common variants associated_with body mass index — 1
common variants associated_with body weight — 1
common variants regulates candidate genes — 1
common variants associated_with candidate genes 0.05 2
common variants associated_with cannabis initiation — 1
common variants risk_factor_for cannabis use — 1
common variants expressed_in cerebellum — 1
common variants associated_with cognitive ability — 1
common variants risk_factor_for complex diseases — 2
common variants associated_with complex diseases — 2
common variants risk_factor_for complex disorders — 1
common variants associated_with complex disorders — 1
common variants associated_with Crohn’s disease — 1
common variants associated_with Cz — 1
common variants associated_with delta power — 1
common variants associated_with depression — 1
common variants associated_with diabetes — 1
common variants risk_factor_for disease — 1
common variants associated_with disease — 1
common variants risk_factor_for disease risk — 1
common variants associated_with disorder — 2
common variants risk_factor_for disorder — 1
common variants associated_with endophenotype — 1
common variants associated_with European ancestry — 2
common variants associated_with European population — 1
common variants associated_with exfoliation glaucoma — 1
common variants risk_factor_for externalizing disorders — 1
common variants expressed_in frontal cortex — 1
common variants risk_factor_for genetic risk — 1
common variants associated_with genetic variants — 1
common variants associated_with height — 4
common variants biomarker_for height — 1
common variants associated_with intellectual disability — 1
common variants associated_with major depressive disorder — 2
common variants regulates miRNA — 1
common variants associated_with mood disorders — 1
common variants risk_factor_for mood disorders — 1
common variants associated_with neuroticism — 2
common variants risk_factor_for nicotine — 1
common variants risk_factor_for obsessive-compulsive disorder — 2
common variants risk_factor_for OCD — 2
common variants associated_with OCD — 1
common variants associated_with P3 amplitude — 1
common variants expressed_in parietal cortex — 1
common variants associated_with phenotype — 1
common variants regulates phenotype — 1
common variants risk_factor_for psychiatric disorders — 7
common variants associated_with psychiatric disorders — 1
common variants associated_with psychiatric traits — 1
common variants interacts_with rare variant — 2
common variants associated_with rare variant — 1
common variants interacts_with rare variation — 1
common variants risk_factor_for schizophrenia — 9
common variants associated_with schizophrenia — 4
common variants associated_with sex — 1
common variants risk_factor_for smoking behavior — 1
common variants associated_with smoking behavior — 1
common variants associated_with smoking cessation 0.0003 1
common variants associated_with smoking quantity 6e-20 1
common variants associated_with SNP — 1
common variants associated_with SNVs — 1
common variants associated_with social cognition — 1
common variants risk_factor_for substance use — 1
common variants associated_with theta band — 1
common variants associated_with theta oscillations — 1
common variants associated_with tobacco initiation — 1
common variants associated_with trait — 1
common variants associated_with type 2 diabetes — 1
common variants associated_with vertex — 1
common variants risk_factor_for vulnerability — 1
ENCODE project targets common variants — 1
European ancestry associated_with common variants — 2
HapMap targets common variants — 1
HapMap associated_with common variants — 1
Illumina HumanHap300 Beadchip targets common variants — 1
inbred strains associated_with common variants — 1
International Hapmap Project associated_with common variants — 1
laboratory mouse interacts_with common variants — 1
PGC meta-analysis interacts_with common variants — 1
rare variant associated_with common variants — 2
rare variant interacts_with common variants — 1
schizophrenia associated_with common variants — 1
SNP associated_with common variants — 2
SNP targets common variants — 1

Mentioned in (119)

Papers in which this entity is mentioned.

Merged raw entities (38)

All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.

Raw name Type Papers Mentions
common variants variant 60 87
common variant variant 34 47
common snps variant 27 43
common genetic variants variant 19 21
common genetic variation variant 6 8
common snp variant 5 8
common genetic variant variant 4 4
common alleles variant 3 3
common dna variants variant 2 2
common genetic factor phenotype 2 2
543 common snps (maf ≥ 0.05) cohort — —
all common snps cohort — —
common alleles cohort — —
common disease associated variant cohort — —
common-disease/common-variant cohort — —
common genetic variants cohort — —
common genetic variation cohort — —
common gene variant cohort — —
common, genome-wide snps cohort — —
common loci cohort — —
common single nucleotide polymorphism cohort — —
common single nucleotide polymorphisms cohort — —
common snp cohort — —
common snps cohort — —
common snps of small effect cohort — —
common variant cohort — —
common variant association cohort — —
common variants cohort — —
common variants (maf >5%) cohort — —
common variation cohort — —
common variations cohort — —
genome-wide snps cohort — —
high-frequency variant cohort — —
highly common variants cohort — —
illumina markers cohort — —
individual common variants cohort — —
maf ≥1% variants cohort — —
single nucleotide polymorphisms cohort — —