"Genetic Services Laboratory, University of Chicago"[submitter] AND "F - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1336198	NM_012280.4(FTSJ1):c.366C>A (p.Thr122=)	FTSJ1	Single nucleotide variant (synonymous variant +1 more)	not specified +1 more	GUncertain significance
Select item 129119	NM_012280.4(FTSJ1):c.495C>T (p.Leu165=)	FTSJ1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 129117	NM_012280.4(FTSJ1):c.572-8C>T	FTSJ1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 129118	NM_012280.4(FTSJ1):c.762A>G (p.Leu254=)	FTSJ1	Single nucleotide variant (synonymous variant)	not provided	GConflicting classifications of pathogenicity
Select item 1336251	NM_012280.4(FTSJ1):c.786C>T (p.Tyr262=)	FTSJ1	Single nucleotide variant (synonymous variant)	not specified	GUncertain significance
Select item 975239	NM_012280.4(FTSJ1):c.*8C>T	FTSJ1	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GLikely benign

ClinVar