"FBXO28-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3040966	NM_015176.4(FBXO28):c.-1G>C	FBXO28, LOC129932579	Single nucleotide variant (5 prime UTR variant +1 more)	FBXO28-related condition	GLikely benign
Select item 2633683	NM_015176.4(FBXO28):c.20A>T (p.Glu7Val)	FBXO28, LOC129932579 (E7V)	Single nucleotide variant (missense variant +1 more)	FBXO28-related condition	GUncertain significance
Select item 2635112	NM_015176.4(FBXO28):c.62G>A (p.Gly21Asp)	FBXO28 (G21D)	Single nucleotide variant (missense variant +1 more)	FBXO28-related condition	GUncertain significance
Select item 3061245	NM_015176.4(FBXO28):c.516+4A>T	FBXO28	Single nucleotide variant (intron variant)	FBXO28-related condition	GUncertain significance
Select item 3044320	NM_015176.4(FBXO28):c.553A>G (p.Asn185Asp)	FBXO28 (N185D)	Single nucleotide variant (missense variant +2 more)	FBXO28-related condition	GUncertain significance
Select item 3048245	NM_015176.4(FBXO28):c.709C>T (p.Pro237Ser)	FBXO28 (P237S)	Single nucleotide variant (missense variant +2 more)	FBXO28-related condition	GLikely benign

ClinVar