"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "ARHGEF7 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 748152	NM_001354046.2(ARHGEF7):c.40C>T (p.Leu14=)	ARHGEF7, ARHGEF7-AS2	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign
Select item 749238	NM_001354046.2(ARHGEF7):c.85G>A (p.Gly29Ser)	ARHGEF7, ARHGEF7-AS2 (G29S)	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign