"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "ARRDC5"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2649083	NM_001080523.3(ARRDC5):c.150C>T (p.Val50=)	ARRDC5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2518841	NM_001048201.3(UHRF1):c.-10-23G>T	ARRDC5, UHRF1 (V3F)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity