ClinVar for MedGen (Select 416) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 598984	NM_001291303.3(FAT4):c.8588T>C (p.Phe2863Ser)	FAT4 (F2863S +1 more)	Single nucleotide variant (missense variant)	Hydrops fetalis +6 more	GUncertain significance
Select item 514535	NM_001291303.3(FAT4):c.11693C>T (p.Ala3898Val)	FAT4 (A3896V +1 more)	Single nucleotide variant (missense variant)	Right ventricular hypertrophy +8 more	GBenign/Likely benign