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. 2019 Jun 21;9:9038. doi: 10.1038/s41598-019-44987-6

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© The Author(s) 2019

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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(A) Bar graph comparing the frequencies of rare JPH2 variants in ostensibly healthy individuals. The gnomAD cohort is broken down into 8 ethnic subgroups. GME Variome and Iranome represent 2 independent Middle Eastern cohorts. No fill, total frequency; tan, missense variant frequency; red, LOF variant frequency. Error bars denote 95% CI; *P < 0.05, **P < 0.001 compared to European (Non-Finnish). (B) Bar graph comparing the frequencies of JPH2 variants in a GME Healthy Cohort (GME Variome + Iranome), an ostensibly healthy population (gnomAD), a cohort of clinical WES referrals at Baylor College of Medicine (WES), a cohort of clinical WES referrals from Iran (WES-Iran), and a population of those diagnosed with HCM. Error bars denote 95% CI; *P < 0.05, **P < 0.001 compared to gnomAD.