"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "DCST2"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2639390	NM_144622.3(DCST2):c.1383C>T (p.Tyr461=)	DCST2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2639391	NM_144622.3(DCST2):c.1152C>T (p.His384=)	DCST2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 493594	GRCh37/hg19 1q21.3-23.1(chr1:153751465-156660462)x3	ADAR, PYGO2 +91 more	Copy number gain	not provided	GLikely pathogenic

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