ClinVar Miner

List of variants reported as likely pathogenic for Congenital stationary night blindness by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000843.4(GRM6):c.2041C>T (p.Gln681Ter)	rs769355168	0.00001
NC_000017.11:g.38339517_38339521delinsGTAGATCA	rs886043488
NM_001004334.4(GPR179):c.2706_2707dup (p.Pro903fs)	rs1200683561

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