Number of variants in six BRCA risk genes in the 1000GP cohort before introduction of risk variants from ClinVar and HGMD (counting only rare coding or splicing variants with CADD > 10).

Susak, Hana; Serra-Saurina, Laura; Demidov, German; Rabionet, Raquel; Domènech, Laura; Bosio, Mattia; Muyas, Francesc; Estivill, Xavier; Escaramís, Geòrgia; Ossowski, Stephan

doi:10.1371/journal.pcbi.1007784.s010

pcbi.1007784.s010.docx (56.19 kB)

Number of variants in six BRCA risk genes in the 1000GP cohort before introduction of risk variants from ClinVar and HGMD (counting only rare coding or splicing variants with CADD > 10).

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posted on 2021-02-19, 19:13 authored by Hana Susak, Laura Serra-Saurina, German Demidov, Raquel Rabionet, Laura Domènech, Mattia Bosio, Francesc Muyas, Xavier Estivill, Geòrgia Escaramís, Stephan Ossowski

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EHMT semi-synthetic whole-exome sequenci...candidate predisposition genes variant association studies BATI phenotypic variance variant Association Test RVAS tests Integrated Nested Laplace Approximation rvGWAS 7A Chronic Lymphocytic Leukemia study COPS

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Number of variants in six BRCA risk genes in the 1000GP cohort before introduction of risk variants from ClinVar and HGMD (counting only rare coding or splicing variants with CADD > 10).

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