"Centogene AG - the Rare Disease Company"[submitter] AND "DISP1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1334043	NM_001377229.1(DISP1):c.566C>T (p.Pro189Leu)	DISP1 (P189L)	Single nucleotide variant (5 prime UTR variant +1 more)	Microform holoprosencephaly	GUncertain significance
Select item 1334044	NM_001377229.1(DISP1):c.664G>A (p.Gly222Ser)	DISP1 (G222S)	Single nucleotide variant (5 prime UTR variant +1 more)	Microform holoprosencephaly	GUncertain significance