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Additional file 8: Figure S4. of Deep targeted sequencing of 12 breast cancer susceptibility regions in 4611 women across four different ethnicities

Year: 2016

Type: article

Abstract: MAF distribution for SNVs observed in this study but not in the 1000 Genomes Project. SNVs observed in this study but not in the 1000 Genomes Project were almost exclusively very rare (MAF <0.005), and only 0.4 % (390 variants) of SNVs not observed in the 1000 Genomes Project had a MAF >0.005 compared with 46 % (17,160) of variants observed in the 1000 Genomes Project. (DOCX 54 kb)

Source: Figshare

DOI: 10.6084/m9.figshare.4316288

Authors: LindstrĂśm, Sara, Ablorh, Akweley, Chapman, Brad, Gusev, Alexander, Chen, Gary, Turman, Constance, Eliassen, A., Price, Alkes, Henderson, Brian, Marchand, Loic Le, Hofmann, Oliver, Haiman, Christopher, Kraft, Peter

Language: English

Topic: BRCA gene mutations in cancer

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDGs: Good health and well-being, Reduced inequalities

Open Access status: green

OpenAlex ID: W7138194038

FWCI:

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