List of variants in gene ELMO2 reported as likely benign for cardiovascular organ benign neoplasm

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_133171.5(ELMO2):c.1416+9C>G	rs770529533	0.00002
NM_133171.5(ELMO2):c.1279+19del	rs76979752

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