C5231416[trait identifier] AND "Human Genetics Bochum, Ruhr University - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2583144	NM_005052.3(RAC3):c.86C>G (p.Pro29Arg)	RAC3 (P29R)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies	GLikely pathogenic
Select item 3025234	NM_005052.3(RAC3):c.277G>A (p.Val93Ile)	RAC3 (V93I)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies +1 more	GConflicting classifications of pathogenicity