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

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 9641	NC_012920.1(MT-ATP6):m.8993T>G	MT-ATP6, MT-ATP8 +24 more	Single nucleotide variant	Mitochondrial disease	GPathogenic FDA Recognized database
Select item 523304	NC_012920.1(MT-ND4):m.11360A>G	MT-ND4	Single nucleotide variant	Seizure +2 more	GUncertain significance
Select item 523305	NC_012920.1:m.11443A>C	MT-ND4	Single nucleotide variant	Visual impairment +4 more	GUncertain significance

Format

Sort by

Choose Destination