"TFAM-related disorder"[Disease/phenotype] AND "PreventionGenetics, pa - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 670994	NM_003201.3(TFAM):c.35G>C (p.Ser12Thr)	TFAM (S12T)	Single nucleotide variant (missense variant +1 more)	TFAM-related disorder +1 more	GBenign
Select item 3053130	NM_003201.3(TFAM):c.102-6A>G	TFAM	Single nucleotide variant (intron variant)	TFAM-related disorder	GLikely benign
Select item 3034666	NM_003201.3(TFAM):c.186A>G (p.Lys62=)	TFAM	Single nucleotide variant (synonymous variant +1 more)	TFAM-related disorder	GLikely benign
Select item 2043897	NM_003201.3(TFAM):c.291+9A>G	TFAM	Single nucleotide variant (intron variant)	TFAM-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 1223044	NM_003201.3(TFAM):c.292-9dup	TFAM	Duplication (intron variant)	TFAM-related disorder +1 more	GBenign
Select item 3046845	NM_003201.3(TFAM):c.633T>C (p.Tyr211=)	TFAM	Single nucleotide variant (synonymous variant +1 more)	TFAM-related disorder	GLikely benign

ClinVar