TNXB and Ehlers-Danlos syndrome: The TNXB variant within Family G (TNXB:NM_019105:exon24:c.C8192G:p.P2731R) appeared in the Leiden Open Variation Database for EDS but was predicted as “benign” (https://databases.lovd.nl/shared/variants/0000313458#00021614, accessed on 4 May 2021).