"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "RNF2"[gene - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2639639	NM_007212.4(RNF2):c.24C>T (p.Asn8=)	RNF2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1335004	NM_007212.4(RNF2):c.734C>T (p.Thr245Met)	RNF2 (T245M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2639640	NM_007212.4(RNF2):c.966C>T (p.Asn322=)	RNF2	Single nucleotide variant (synonymous variant)	not provided	GBenign

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