C3809609[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 1333734	NM_001128840.3(CACNA1D):c.4863A>T (p.Lys1621Asn)	CACNA1D (K1606N +2 more)	Single nucleotide variant (missense variant)	Aldosterone-producing adenoma with seizures and neurological abnormalities	GUncertain significance
Select item 1333735	NM_001128840.3(CACNA1D):c.5587C>T (p.Gln1863Ter)	CACNA1D (Q1839* +2 more)	Single nucleotide variant (nonsense)	Aldosterone-producing adenoma with seizures and neurological abnormalities	GUncertain significance