C1848029[trait identifier] AND "Centogene AG - the Rare Disease Compan - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1325212	NM_001365276.2(TNXB):c.8473G>A (p.Glu2825Lys)	TNXB (E2825K)	Single nucleotide variant (missense variant +1 more)	Vesicoureteral reflux 8 +1 more	GLikely pathogenic
Select item 1333728	NM_001365276.2(TNXB):c.1739A>G (p.Tyr580Cys)	TNXB (Y580C)	Single nucleotide variant (missense variant)	Vesicoureteral reflux 8 +2 more	GUncertain significance