"Centogene AG - the Rare Disease Company"[submitter] AND "TMEM260"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 974872	NM_017799.4(TMEM260):c.1688del (p.Thr563fs)	TMEM260 (T563fs)	Deletion (frameshift variant)	Structural heart defects and renal anomalies syndrome	GLikely pathogenic
Select item 426076	NM_017799.4(TMEM260):c.1698_1701del (p.Tyr567fs)	TMEM260 (Y567fs)	Deletion (frameshift variant)	Structural heart defects and renal anomalies syndrome	GPathogenic