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101 patients (28.4%) had at least one genetic variant, and 9 patients with variants in more than one gene were identified

Bari I, Erdol S, Saglam H, Lovri M, Belui R, Vugrek O, Blom HJ, Fumi K (2017b) Glycine N-methyltransferase deficiency: A member of dysmethylating liver disorders

Unless you are recovering from macrocytic anaemia (or you've recently lost a lot of weight) you shouldn't need extra potassium

Unlike GHRP-6 and GHRP-2, Ipamorelin stimulates GH release without meaningfully elevating cortisol, prolactin, or ACTH at physiological doses (PMID: 9849822)