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Frequency of familial hypercholesterolaemia-causing genetic variants in the 100 000 Genomes Project cohort: whole genome sequencing analyses of 77 260 participants

jmedgenet · abstract · 2026-04-20 · 3 matching annotations

79.2%

100 000 Genomes Project 100KGP HeFH cancer

…scular risk. In the UK, HeFH affects ~1 in 288 individuals. The 100 000 Genomes Project (100KGP) generated whole genome sequencing (WGS) data from >85 …

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100KGP

Articles mentioning 100KGP

Frequency of familial hypercholesterolaemia-causing genetic variants in the 100 000 Genomes Project cohort: whole genome sequencing analyses of 77 260 participants