ClinVar Miner

List of variants reported as likely pathogenic for cone-rod dystrophy 9

Included ClinVar conditions (1):

Cone-rod dystrophy 9

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_003816.3(ADAM9):c.103C>T (p.Gln35Ter)
NM_003816.3(ADAM9):c.1616del (p.Cys539fs)
NM_003816.3(ADAM9):c.1698-1715_1881+156del
NM_003816.3(ADAM9):c.576del (p.Glu193fs)	rs2129433190

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