List of variants in gene SEC24D reported as likely pathogenic 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_014822.4(SEC24D):c.1055T>A (p.Leu352Ter)
NM_014822.4(SEC24D):c.1724G>C (p.Gly575Ala)
NM_014822.4(SEC24D):c.958C>T (p.Pro320Ser)

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