NM_004713.6:c.1234_1235insC

Subject ID	Country of Origin	Allele Count	Allele Frequency	CTGA Clinical Significance	Condition(s)	Reference	Remarks
619099.5.1	Saudi Arabia	2	NA	Pathogenic	Intellectual Developmental Disorder with Speech Delay and Axonal Peripheral Neuropathy	Ahmed et al. 2021	Patient from 'family 4' in the publicati...
619099.5.2	Saudi Arabia	1	NA			Ahmed et al. 2021	Father of 619099.5.1
619099.5.3	Saudi Arabia	1	NA			Ahmed et al. 2021	Mother of 619099.5.1
619099.6.1	Saudi Arabia	2	NA	Pathogenic	Intellectual Developmental Disorder with Speech Delay and Axonal Peripheral Neuropathy	Ahmed et al. 2021	Patient from 'family 5' in the publicati...
619099.6.2	Saudi Arabia	1	NA			Ahmed et al. 2021	Father of 619099.6.1
619099.6.3	Saudi Arabia	1	NA			Ahmed et al. 2021	Mother of 619099.6.1

Epidemiology in the Arab World