ClinVar Miner

List of variants in gene RNASEH1 reported as benign for adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy

Included ClinVar conditions (1):

Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_002936.6(RNASEH1):c.409+34C>A	rs7563960	0.69067
NM_002936.6(RNASEH1):c.498A>G (p.Pro166=)	rs10186193	0.41265

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