Sökning: WFRF:(Makela T. P.) > (2020-2024) > FinnGen provides ge...
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001 | oai:prod.swepub.kib.ki.se:151978389 | |
003 | SwePub | |
008 | 240701s2023 | |||||||||||000 ||eng| | |
024 | 7 | a http://kipublications.ki.se/Default.aspx?queryparsed=id:1519783892 URI |
024 | 7 | a https://doi.org/10.1038/s41586-022-05473-82 DOI |
040 | a (SwePub)ki | |
041 | a engb eng | |
042 | 9 SwePub | |
072 | 7 | a ref2 swepub-contenttype |
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100 | 1 | a Kurki, MI4 aut |
245 | 1 0 | a FinnGen provides genetic insights from a well-phenotyped isolated population |
264 | c 2023-01-18 | |
264 | 1 | b Springer Science and Business Media LLC,c 2023 |
520 | a Population isolates such as those in Finland benefit genetic research because deleterious alleles are often concentrated on a small number of low-frequency variants (0.1% ≤ minor allele frequency < 5%). These variants survived the founding bottleneck rather than being distributed over a large number of ultrarare variants. Although this effect is well established in Mendelian genetics, its value in common disease genetics is less explored1,2. FinnGen aims to study the genome and national health register data of 500,000 Finnish individuals. Given the relatively high median age of participants (63 years) and the substantial fraction of hospital-based recruitment, FinnGen is enriched for disease end points. Here we analyse data from 224,737 participants from FinnGen and study 15 diseases that have previously been investigated in large genome-wide association studies (GWASs). We also include meta-analyses of biobank data from Estonia and the United Kingdom. We identified 30 new associations, primarily low-frequency variants, enriched in the Finnish population. A GWAS of 1,932 diseases also identified 2,733 genome-wide significant associations (893 phenome-wide significant (PWS), P < 2.6 × 10–11) at 2,496 (771 PWS) independent loci with 807 (247 PWS) end points. Among these, fine-mapping implicated 148 (73 PWS) coding variants associated with 83 (42 PWS) end points. Moreover, 91 (47 PWS) had an allele frequency of <5% in non-Finnish European individuals, of which 62 (32 PWS) were enriched by more than twofold in Finland. These findings demonstrate the power of bottlenecked populations to find entry points into the biology of common diseases through low-frequency, high impact variants. | |
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710 | 2 | a Karolinska Institutet4 org |
773 | 0 | t Natured : Springer Science and Business Media LLCg 613:7944, s. 508-+q 613:7944<508-+x 1476-4687x 0028-0836 |
856 | 4 8 | u http://kipublications.ki.se/Default.aspx?queryparsed=id:151978389 |
856 | 4 8 | u https://doi.org/10.1038/s41586-022-05473-8 |
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