List of variants in gene combination LOC130006028, LTBP3 reported as uncertain significance for Brachyolmia-amelogenesis imperfecta syndrome

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001130144.3(LTBP3):c.2854G>A (p.Asp952Asn)	rs756826691	0.00001
NM_001130144.3(LTBP3):c.2846G>A (p.Gly949Asp)
NM_001130144.3(LTBP3):c.2852G>T (p.Gly951Val)

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