"PreventionGenetics, part of Exact Sciences"[submitter] AND "FBXO7"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3033374	NM_012179.4(FBXO7):c.122+245G>A	FBXO7 (R3Q)	Single nucleotide variant (missense variant +2 more)	FBXO7-related condition	GLikely benign
Select item 2635086	NM_012179.4(FBXO7):c.131C>A (p.Thr44Asn)	FBXO7 (T44N)	Single nucleotide variant (5 prime UTR variant +2 more)	FBXO7-related condition	GUncertain significance
Select item 1907641	NM_012179.4(FBXO7):c.595T>C (p.Leu199=)	FBXO7	Single nucleotide variant (synonymous variant)	Parkinsonian-pyramidal syndrome +1 more	GLikely benign
Select item 341312	NM_012179.4(FBXO7):c.693C>T (p.Ser231=)	FBXO7	Single nucleotide variant (synonymous variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 631890	NM_012179.4(FBXO7):c.726_727del (p.Cys243fs)	FBXO7 (C164fs +2 more)	Microsatellite (frameshift variant)	Parkinsonian-pyramidal syndrome +2 more	GConflicting classifications of pathogenicity
Select item 444586	NM_012179.4(FBXO7):c.1546G>C (p.Asp516His)	FBXO7 (D516H +2 more)	Single nucleotide variant (missense variant)	FBXO7-related condition +2 more	GConflicting classifications of pathogenicity

ClinVar