Related gene-specific medical variations for Gene (Select 5983) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685460	GRCh37/hg19 13q13.2(chr13:34355904-34420138)x1	RFC3	Copy number loss	not provided	GUncertain significance
Select item 564022	GRCh37/hg19 13q13.2(chr13:34347960-34642138)x3	RFC3	Copy number gain	not provided	GUncertain significance
Select item 563993	GRCh37/hg19 13q13.2(chr13:34460725-34522513)x1	RFC3	Copy number loss	not provided	GLikely benign
Select item 242955	t(7;13)(q31.1;q13.2)	RFC3, FOXP2	Translocation	Childhood apraxia of speech	GPathogenic

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