List of variants in gene LTBP2 reported as uncertain significance for Primary congenital glaucoma

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000428.3(LTBP2):c.3753C>T (p.Ser1251=)	rs763990884	0.00008
NM_000428.3(LTBP2):c.*1743C>T	rs781717691	0.00006
NM_000428.3(LTBP2):c.*10dup	rs546442756
NM_000428.3(LTBP2):c.1518_1520dup	rs565536636

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