Additional file 5 of Identification of novel MYO19 variants in neonatal hypertrophic cardiomyopathy: a familial analysis revealing oligogenic contributors to disease severity
Category of significance (“very high” “High”,“Medium”) as defined below: *represents known pseudogene; Chr chromosome. “High” p<0.00044 (based on p-value which reaches genome-wide significance if repl
This dataset consists of scanning electron microscopy (SEM) measurements and sequencing data of two population specific variants; rs11150606 (chr16:g.31087690T>C (hg38) p.Gln30Arg) observed in East
