Figure 1 | Scientific Reports

Figure 1

From: An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort

Figure 1

Extracts from two multi-generational VIKING pedigrees. (A) Excerpt from a pedigree containing more than 30 genotyped participants, Family A. The initial participant with WGS (ID1) is indicated by an arrow and his two carrier relatives (ID2 and ID3) in the pedigree are shaded in black. (B) Excerpt from a second pedigree (Family B) containing 10 genotyped participants. The two participants identified by haplotype analysis, ID4 and ID5, are shaded in black. Other genotyped VIKING participants in each family are shown in green, and participants with WGS data are indicated. Family members not in the research cohort are represented in lighter shading. There are many other family members not shown. Obligate carriers of the rare variant are filled in dark grey. Values below each individual are their measured QTc interval.

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