ClinVar Miner

List of variants reported as likely benign for Cataract 1 multiple types; Chromosome 1q21.1 deletion syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_005267.5(GJA8):c.658A>G (p.Asn220Asp)	rs138140155	0.00247

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