2014
DOI: 10.1186/1471-2164-15-437
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Population-specific common SNPs reflect demographic histories and highlight regions of genomic plasticity with functional relevance

Abstract: BackgroundPopulation differentiation is the result of demographic and evolutionary forces. Whole genome datasets from the 1000 Genomes Project (October 2012) provide an unbiased view of genetic variation across populations from Europe, Asia, Africa and the Americas. Common population-specific SNPs (MAF > 0.05) reflect a deep history and may have important consequences for health and wellbeing. Their interpretation is contextualised by currently available genome data.ResultsThe identification of common populati… Show more

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Cited by 42 publications
(31 citation statements)
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“…We report evidence for an association of both common and low‐frequency SLC2A3 variants with ADHD. While SNP rs12842, which tags almost the entire SLC2A3 region, was replicably associated with ADHD across several European samples, the SLC2A3 duplication reached significance only in the German cohort, suggesting population‐specificity of the SLC2A3 CNV‐linked disease risk (Choudhury et al., ). This is further supported by the notion that rs12842 tags synthetic association with a functional CNV (Kent, ), and also confers risk independently.…”
Section: Discussionmentioning
confidence: 99%
“…We report evidence for an association of both common and low‐frequency SLC2A3 variants with ADHD. While SNP rs12842, which tags almost the entire SLC2A3 region, was replicably associated with ADHD across several European samples, the SLC2A3 duplication reached significance only in the German cohort, suggesting population‐specificity of the SLC2A3 CNV‐linked disease risk (Choudhury et al., ). This is further supported by the notion that rs12842 tags synthetic association with a functional CNV (Kent, ), and also confers risk independently.…”
Section: Discussionmentioning
confidence: 99%
“…These regions seem to coincide with recombination hotspots (Chimusa et al, 2015). Very few of these recombination hotspots seem to be shared between African and other populations (Choudhury et al, 2014;Chimusa et al, 2015). Perhaps the high variability of the SMN region in the black SA population could be due to frequent recombination events in the SMN region.…”
Section: Challenges and Limitations Of The Studymentioning
confidence: 92%
“…For this SNP, we detected a lower T allele frequency in control group (0.105) in comparison to the one stated in 1000 Genomes database (Caucasians/European/Iberian population in Spain: 0.402; P < 0.001). Global diversity of human genome is the outcome of a series of demographic and evolutionary events (such as admixture, population isolation, and genetic drift), which occurred in different parts of the world at various time points in history . This fact may explain, at least, the allele frequency of DNMT3A SNP observed in Portuguese population.…”
Section: Resultsmentioning
confidence: 99%