List of variants in gene MT-RNR1 reported as pathogenic for Mitochondrial non-syndromic sensorineural hearing loss

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: 4

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.1095T>C	rs267606618
NC_012920.1(MT-CYB):m.961T>G	rs3888511
NC_012920.1:m.827A>G	rs28358569
m.1291T>C	rs267606620

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