ClinVar Miner

List of variants reported for Autosomal recessive nonsyndromic hearing loss 31; Usher syndrome type 2D by Division of Human Genetics, Children's Hospital of Philadelphia

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_015404.4(WHRN):c.191C>A (p.Ala64Asp)	rs146655362	0.00053
NM_015404.4(WHRN):c.2569C>T (p.Gln857Ter)	rs727504817

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