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- Common_disease-common_variant abstract "The common disease-common variant (often abbreviated CD-CV) hypothesis predicts that common disease-causing alleles, or variants, will be found in all human populations which manifest a given disease. Common variants (not necessarily disease-causing) are known to exist in coding and regulatory sequences of genes. According to the CD-CV hypothesis, some of those variants lead to susceptibility to complex polygenic diseases. Each variant at each gene influencing a complex disease will have a small additive or multiplicative effect on the disease phenotype. These diseases, or traits, are evolutionarily neutral in part because so many genes influence the traits. The hypothesis has held true in the case of putative causal variants in apolipoprotein E, including APOE ε4, associated with Alzheimer's disease. IL23R has been found to be associated with Crohn's disease; the at-risk allele has a frequency 93% in the general population.One common form of variation across human genomes is called a single nucleotide polymorphism (SNP). As indicated by the name, SNPs are single base changes in the DNA. SNP variants tend to be common in different human populations. These polymorphisms have been valuable as genomic signposts, or \"markers,\" in the search for common variants that influence susceptibility to common diseases. Recently published research has linked common SNPs to diseases such as type 2 diabetes, Alzheimer's, schizophrenia and hypertension.".
- Common_disease-common_variant wikiPageID "8476844".
- Common_disease-common_variant wikiPageLength "8697".
- Common_disease-common_variant wikiPageOutDegree "9".
- Common_disease-common_variant wikiPageRevisionID "699104498".
- Common_disease-common_variant wikiPageWikiLink Alzheimers_disease.
- Common_disease-common_variant wikiPageWikiLink Apolipoprotein.
- Common_disease-common_variant wikiPageWikiLink Category:Genetics.
- Common_disease-common_variant wikiPageWikiLink Category:Medical_research.
- Common_disease-common_variant wikiPageWikiLink Category:Race_and_health.
- Common_disease-common_variant wikiPageWikiLink Crohns_disease.
- Common_disease-common_variant wikiPageWikiLink Interleukin-23_receptor.
- Common_disease-common_variant wikiPageWikiLink Rare_functional_variant.
- Common_disease-common_variant wikiPageWikiLink Single-nucleotide_polymorphism.
- Common_disease-common_variant wikiPageWikiLinkText ""common disease-common variant"".
- Common_disease-common_variant wikiPageWikiLinkText "Common disease-common variant".
- Common_disease-common_variant wikiPageWikiLinkText "common disease-common variant (CD/CV) hypothesis".
- Common_disease-common_variant wikiPageWikiLinkText "common disease/common variant".
- Common_disease-common_variant wikiPageWikiLinkText "common variants".
- Common_disease-common_variant wikiPageUsesTemplate Template:Citation_needed.
- Common_disease-common_variant wikiPageUsesTemplate Template:Reflist.
- Common_disease-common_variant subject Category:Genetics.
- Common_disease-common_variant subject Category:Medical_research.
- Common_disease-common_variant subject Category:Race_and_health.
- Common_disease-common_variant type Determinant.
- Common_disease-common_variant type Factor.
- Common_disease-common_variant comment "The common disease-common variant (often abbreviated CD-CV) hypothesis predicts that common disease-causing alleles, or variants, will be found in all human populations which manifest a given disease. Common variants (not necessarily disease-causing) are known to exist in coding and regulatory sequences of genes. According to the CD-CV hypothesis, some of those variants lead to susceptibility to complex polygenic diseases.".
- Common_disease-common_variant label "Common disease-common variant".
- Common_disease-common_variant sameAs Q5153533.
- Common_disease-common_variant sameAs m.0274wqd.
- Common_disease-common_variant sameAs Q5153533.
- Common_disease-common_variant wasDerivedFrom Common_disease-common_variant?oldid=699104498.
- Common_disease-common_variant isPrimaryTopicOf Common_disease-common_variant.