"Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, E - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 784732	NM_001421.4(ELF4):c.1810C>T (p.Arg604Cys)	ELF4 (R604C)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1328021	NM_001421.4(ELF4):c.1144G>A (p.Val382Ile)	ELF4 (V382I)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1206203	NM_001421.4(ELF4):c.810-4C>G	ELF4	Single nucleotide variant (intron variant)	not provided	GLikely benign

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