Related gene-specific medical variations for Gene (Select 222234) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2524332	NM_001394494.2(FBXL13):c.2474C>T (p.Ala825Val)	FAM185A, FBXL13 (A825V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2493137	NM_001394494.2(FBXL13):c.2401A>G (p.Asn801Asp)	FAM185A, FBXL13 (N683D +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2455849	NM_001394494.2(FBXL13):c.2252G>A (p.Arg751Gln)	FAM185A, FBXL13 (R633Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2249146	NM_001394494.2(FBXL13):c.2320C>A (p.Gln774Lys)	FAM185A, FBXL13 (Q684K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2240921	NM_001394494.2(FBXL13):c.2153C>T (p.Ser718Leu)	FAM185A, FBXL13 (S600L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208197	NM_001394494.2(FBXL13):c.2148G>A (p.Met716Ile)	FAM185A, FBXL13 (M581I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar