"Genome-Nilou Lab"[submitter] AND "ELN"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 213163	NM_000501.4(ELN):c.1315+17C>T	ELN	Single nucleotide variant (intron variant)	not specified +3 more	GBenign
Select item 1249499	NM_000501.4(ELN):c.1414+24C>T	ELN	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 177898	NM_000501.4(ELN):c.1741G>C (p.Gly581Arg)	ELN-AS1, ELN (G581R +11 more)	Single nucleotide variant (missense variant)	not specified +4 more	GBenign/Likely benign

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