List of variants in gene LTBP3 reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NC_000011.10:g.65558454G>T	rs7927077	0.76081
NM_001130144.3(LTBP3):c.971-53C>T	rs4244811	0.58853
NM_001130144.3(LTBP3):c.1531+178A>G	rs11227221	0.58784
NM_001130144.3(LTBP3):c.2107+80T>A	rs58621819	0.17164
NM_001130144.3(LTBP3):c.2597-133dup	rs77639728	0.05510
NM_001130144.3(LTBP3):c.2107+8G>A	rs74202491	0.05179
NM_001130144.3(LTBP3):c.1313C>T (p.Ala438Val)	rs11545200	0.05087
NM_001130144.3(LTBP3):c.2107+90_2107+91del	rs199773504	0.04921
NM_001130144.3(LTBP3):c.2107+62G>A	rs77880196	0.04821
NC_000011.10:g.65558451T>G	rs184216483	0.04401
NM_001130144.3(LTBP3):c.-30C>T	rs192543645	0.03496
NM_001130144.3(LTBP3):c.3548-9T>C	rs149115544	0.00259
NC_000011.10:g.65558453T>G	rs767332175
NM_001130144.3(LTBP3):c.*195C>T	rs11545201
NM_001130144.3(LTBP3):c.2107+95del	rs58373954
NM_001130144.3(LTBP3):c.2596+130ATCC[10]	rs140563368
NM_001130144.3(LTBP3):c.2596+130ATCC[12]	rs140563368
NM_001130144.3(LTBP3):c.76CTG[11] (p.Leu35dup)	rs71036212
NM_001130144.3(LTBP3):c.76CTG[9] (p.Leu35del)	rs71036212

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