"PreventionGenetics, part of Exact Sciences"[submitter] AND "TFG"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2635406	NM_006070.6(TFG):c.145C>A (p.Leu49Met)	TFG (L49M)	Single nucleotide variant (missense variant)	TFG-related disorder	GUncertain significance
Select item 466406	NM_006070.6(TFG):c.185-10T>C	TFG	Single nucleotide variant (intron variant)	Hereditary motor and sensory neuropathy, Okinawa type +2 more	GBenign/Likely benign
Select item 386659	NM_006070.6(TFG):c.258G>T (p.Leu86=)	TFG	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +4 more	GBenign/Likely benign
Select item 378719	NM_006070.6(TFG):c.416-9T>C	TFG	Single nucleotide variant (intron variant)	Hereditary motor and sensory neuropathy, Okinawa type +4 more	GBenign/Likely benign
Select item 706416	NM_006070.6(TFG):c.581-6A>C	TFG	Single nucleotide variant (intron variant)	Hereditary motor and sensory neuropathy, Okinawa type +2 more	GLikely benign
Select item 466410	NM_006070.6(TFG):c.594T>G (p.Ala198=)	TFG	Single nucleotide variant (synonymous variant)	Hereditary motor and sensory neuropathy, Okinawa type +4 more	GBenign/Likely benign
Select item 378721	NM_006070.6(TFG):c.663C>A (p.Gly221=)	TFG	Single nucleotide variant (synonymous variant)	Hereditary motor and sensory neuropathy, Okinawa type +4 more	GBenign/Likely benign
Select item 3051495	NM_006070.6(TFG):c.722-8del	TFG	Deletion (intron variant)	TFG-related disorder	GLikely benign

ClinVar