ClinVar Miner

List of variants reported as benign for Glaucoma 3, primary infantile, B; Glaucoma 3, primary congenital, D; Weill-Marchesani syndrome 3; Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma by Fulgent Genetics, Fulgent Genetics

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000428.3(LTBP2):c.4888+18G>A	rs73296217	0.01044
NM_000428.3(LTBP2):c.785C>T (p.Pro262Leu)	rs143106228	0.00232

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