"Genome Diagnostics Laboratory, Amsterdam University Medical Center"[s - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 708236	NM_014967.5(FAN1):c.149T>G (p.Met50Arg)	FAN1 (M50R)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome +2 more	GConflicting classifications of pathogenicity
Select item 719369	NM_014967.5(FAN1):c.718G>A (p.Glu240Lys)	FAN1 (E240K)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1218283	NM_014967.5(FAN1):c.1851C>T (p.Ser617=)	FAN1	Single nucleotide variant (synonymous variant)	Karyomegalic interstitial nephritis +1 more	GBenign/Likely benign
Select item 715459	NM_014967.5(FAN1):c.1944-4T>C	FAN1, MTMR10	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 771908	NM_014967.5(FAN1):c.2418C>T (p.Asp806=)	FAN1, MTMR10	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 1200441	NM_014967.5(FAN1):c.2680C>T (p.Pro894Ser)	FAN1, MTMR10 (P894S)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign

ClinVar