ClinVar (all) for Orgtrack (Select 509479) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3066071	NC_012920.1(MT-CYB):m.73A>G		Single nucleotide variant	Venous thromboembolism	GAffects
Select item 3027424	NC_012920.1(MT-ND4):m.11719G>A	MT-ND4	Single nucleotide variant	Venous thromboembolism	Gassociation
Select item 3027423	NC_012920.1(MT-CYB):m.16223C>T		Single nucleotide variant	Venous thromboembolism	Gassociation not found
Select item 3027422	NC_012920.1(MT-ND4):m.12007G>A	MT-ND4	Single nucleotide variant	Venous thromboembolism	GBenign
Select item 3027421	NC_012920.1(MT-CO3):m.9540T>C	MT-CO3	Single nucleotide variant	Venous thromboembolism	GBenign
Select item 441148	NC_012920.1(MT-CYB):m.750A>G	MT-RNR1	Single nucleotide variant	Venous thromboembolism	Gassociation not found
Select item 140589	NC_012920.1(MT-CYB):m.15043G>A	MT-CYB	Single nucleotide variant	Familial cancer of breast	GBenign
Select item 140587	NC_012920.1(MT-CYB):m.14766C>T	MT-CYB	Single nucleotide variant	Leigh syndrome	GBenign

ClinVar