C4014419[trait identifier] AND "Department of Medical Genetics, Oslo U - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 981198	NM_001371928.1(AHDC1):c.3185_3186del (p.Thr1062fs)	AHDC1 (T1062fs)	Microsatellite (frameshift variant)	AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome	GPathogenic
Select item 981199	NM_001371928.1(AHDC1):c.2772del (p.Arg925fs)	AHDC1 (R925fs)	Deletion (frameshift variant)	AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome	GLikely pathogenic