Related gene-specific medical variations for Gene (Select 85449) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2218861	NM_001029864.2(KIAA1755):c.2677G>A (p.Ala893Thr)	KIAA1755, LOC126863025 (A544T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 161499	NM_001029864.2(KIAA1755):c.3089G>T (p.Gly1030Val)	KIAA1755 (G1030V +1 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance