"Centre for Mendelian Genomics, University Medical Centre Ljubljana"[s - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 931874	NM_001256071.3(RNF213):c.1112+6G>A	RNF213	Single nucleotide variant (intron variant)	See cases	GUncertain significance
Select item 930412	NM_001256071.3(RNF213):c.2502-11_2502-10del	RNF213	Deletion (intron variant)	not provided	GUncertain significance
Select item 523426	NM_001256071.3(RNF213):c.11659A>G (p.Lys3887Glu)	RNF213, RNF213-AS1 (K3887E)	Single nucleotide variant (missense variant)	Patent foramen ovale +6 more	GUncertain significance

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