List of variants in gene MT-CO3 reported as pathogenic for congenital anomaly of cardiovascular system

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NC_012920.1:m.9273_9274insATC	rs1569484288
NC_012920.1:m.9429_9430insCCC	rs1569484299
NC_012920.1:m.9441_9442insTTT	rs1569484301

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