Related gene-specific medical variations for Gene (Select 864) - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2688533	NM_001031680.2(RUNX3):c.53T>A (p.Ile18Asn)	RUNX3, RUNX3-AS1 (I18N)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GBenign
Select item 2306562	NM_004350.3(RUNX3):c.1147G>A (p.Gly383Ser)	LOC129929724, RUNX3 (G397S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 774578	NM_001031680.2(RUNX3):c.57C>A (p.Arg19=)	RUNX3, RUNX3-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign

Format

Sort by

Choose Destination

ClinVar