C0002395[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 10	NM_000410.4(HFE):c.187C>G (p.His63Asp)	HFE, HFE-AS1 (H63D +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	Familial porphyria cutanea tarda +9 more	GPathogenic/Likely pathogenic/Pathogenic, low penetrance; other
Select item 1156848	NM_000484.3(APP):c.-626C>T	APP, APP-DT	Single nucleotide variant	not provided +1 more	GConflicting classifications of pathogenicity