ClinVar Miner

List of variants reported as pathogenic for autosomal recessive nonsyndromic hearing loss 2 by The Shared Resource Centre "Genome", Research Centre for Medical Genetics

Included ClinVar conditions (3):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_000260.4(MYO7A):c.3262C>T (p.Gln1088Ter)	rs376535635	0.00001
NM_000260.4(MYO7A):c.5573T>C (p.Leu1858Pro)	rs368657015	0.00001

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