List of variants in gene LTBP4 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001042545.2(LTBP4):c.284T>C (p.Val95Ala)	rs200888669	0.00038
NM_001042545.2(LTBP4):c.4604G>A (p.Cys1535Tyr)	rs200665923	0.00034
NM_001042545.2(LTBP4):c.2176G>C (p.Glu726Gln)	rs199691160	0.00013
NM_001042545.2(LTBP4):c.3368C>T (p.Pro1123Leu)	rs369221693	0.00004
NM_003573.2(LTBP4):c.334G>T (p.Ala112Ser)	rs2081414000

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