"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "RFC2"[gene - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1879690	NM_181471.3(RFC2):c.780A>C (p.Pro260=)	RFC2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2657586	NM_181471.3(RFC2):c.586G>A (p.Ala196Thr)	RFC2 (A162T +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2657587	NM_181471.3(RFC2):c.226-3C>T	RFC2	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign

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