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. Author manuscript; available in PMC: 2022 Jun 1.
Published in final edited form as: Circ Genom Precis Med. 2021 Apr 22;14(3):e003232. doi: 10.1161/CIRCGEN.120.003232

Figure 2.

Figure 2.

Subset of the SAFHS pedigree displaying inheritance of 23 copies of the ANGPTL3 5bp deletion variant rs398122988. This rare loss of function frameshift deletion variant was only detected in this single family. Half-filled symbols are heterozygous carriers of the rs398122988 variant, cross-hatched symbols are individuals for whom WGS data is not available, empty white symbols are individuals who do not carry the variant. Blue highlights indicate individuals with multiple spouses.