List of variants in gene EFTUD2 reported as likely benign for bone development disease

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_004247.4(EFTUD2):c.1058+3_1058+7del	rs536749831	0.00538
NM_004247.4(EFTUD2):c.106-17C>T	rs190562796	0.00020
NM_004247.4(EFTUD2):c.2389G>T (p.Ala797Ser)

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