ANKH and epilepsy: ANKH‐associated epilepsy may be underdiagnosed for two reasons; first, the C>T change is located in the 5′UTR region of the gene, 11 nucleotides upstream of the “normal” translation initiation start‐codon, and second because of the currently missing connection of the ANKH gene entry with a seizure phenotype in relevant databases that are integrated in standard bioinformatic pipelines for variant calling and variant interpretation (e.g., databases like OMIM and ClinVar).