"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "FHL3"[gene - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2638683	NM_004468.5(FHL3):c.789C>T (p.Phe263=)	FHL3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2638684	NM_004468.5(FHL3):c.438T>A (p.Gly146=)	FHL3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2638685	NM_004468.5(FHL3):c.309T>C (p.Ala103=)	FHL3	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign

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