List of variants in gene combination LOC130006030, LTBP3 reported as pathogenic for bone disorder

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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_001130144.3(LTBP3):c.2209del (p.Gln737fs)	rs2496149719
NM_001130144.3(LTBP3):c.2210del (p.Gln737fs)
NM_001130144.3(LTBP3):c.2215_2216delinsT (p.Gly739fs)	rs2496149640
NM_001130144.3(LTBP3):c.2216del (p.Gly739fs)	rs752375653

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