List of variants in gene LEMD3 reported as likely benign by Eurofins NTD LLC (GA)

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_014319.5(LEMD3):c.1746C>T (p.Ile582=)	rs140496862	0.00089
NM_014319.5(LEMD3):c.907G>T (p.Gly303Cys)	rs35221558	0.00085
NM_014319.5(LEMD3):c.2331A>C (p.Ser777=)	rs146896083	0.00058
NM_014319.5(LEMD3):c.240_263del (p.Pro81_Gly88del)	rs756800816

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