List of variants in gene ELMO2 reported as pathogenic for 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_133171.5(ELMO2):c.1065+1G>A	rs768410753	0.00001
NM_133171.5(ELMO2):c.1065+1G>T
NM_133171.5(ELMO2):c.1802-1G>C	rs886037918
NM_133171.5(ELMO2):c.2080del (p.Leu694fs)	rs886037919
NM_133171.5(ELMO2):c.311dup (p.Met104fs)	rs2145827538

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