List of variants in gene ELMO2 reported as likely pathogenic 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_133171.5(ELMO2):c.1447C>T (p.Arg483Ter)	rs1372506599	0.00001
NM_133171.5(ELMO2):c.1525C>T (p.Arg509Ter)	rs1568748859
NM_133171.5(ELMO2):c.1802-1G>C	rs886037918

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