List of variants in gene ELN reported as likely benign for chromosomal disorder

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_000501.4(ELN):c.1909G>A (p.Ala637Thr)	rs536177240	0.00026
NM_000501.4(ELN):c.381G>A (p.Ala127=)	rs148216123	0.00019
NM_000501.4(ELN):c.249C>T (p.Pro83=)	rs565001805	0.00016

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