"Centre for Mendelian Genomics, University Medical Centre Ljubljana"[s - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 931780	NM_001291303.3(FAT4):c.5944A>G (p.Ser1982Gly)	FAT4 (S1982G)	Single nucleotide variant (missense variant)	Hennekam lymphangiectasia-lymphedema syndrome 2	GUncertain significance
Select item 932020	NM_001291303.3(FAT4):c.14404C>T (p.Pro4802Ser)	FAT4 (P4800S +2 more)	Single nucleotide variant (missense variant)	Hennekam lymphangiectasia-lymphedema syndrome 2	GUncertain significance