List of variants in gene ECM1 reported as benign for Lipid proteinosis

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004425.4(ECM1):c.1243G>A (p.Gly415Ser)	rs13294	0.33313
NM_004425.4(ECM1):c.389C>T (p.Thr130Met)	rs3737240	0.29423
NM_004425.4(ECM1):c.792G>A (p.Glu264=)	rs78194273	0.01478
NM_004425.4(ECM1):c.1083+10C>T	rs55770822	0.00336

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