C3810283[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 1333955	NM_006767.4(LZTR1):c.320+1G>C	LZTR1	Single nucleotide variant (splice donor variant)	not provided +4 more	GLikely pathogenic
Select item 967710	NM_006767.4(LZTR1):c.1373dup (p.His459fs)	LZTR1 (H459fs)	Duplication (frameshift variant)	not provided +1 more	GPathogenic/Likely pathogenic