Fig. 2
From: Diagnostic yield of genetic testing in a heterogeneous cohort of 1376 HCM patients
Distribution of Diagnostic Variants by Gene. Bar chart demonstrates the distribution of diagnostic variants by gene as a percentage of total variants (n = 373). The Y axis indicates the percentage of all diagnostic variants (rounded to the nearest whole percent) and the X axis indicates the gene. Section titled “Other” includes genes that had five variants or less detected. Genes with ≤ 5 variants detected: MYL2 (n = 5), PTPN11 (n = 4), DES (n = 3), TTN (n = 3), LMNA (n = 2), FHL1 (n = 2), FLNC (n = 2), HRAS (n = 2), LAMP2 (n = 2), MYL3 (n = 2), PRKAG2 (n = 2), TTR (n = 2), DSG2 (n = 2), CPT2 (n = 1), MAP2K1 (n = 1), SHOC2 (n = 1), ACTC1 (n = 1), PLN (n = 1), TRPM4 (n = 1), JUP (n = 1), NF1 (n = 1), RYR2 (n = 1), SCN5A (n = 1)