ClinVar Miner

List of variants in gene EPCAM reported as pathogenic for Lynch syndrome 8

Included ClinVar conditions (2):

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_002354.3(EPCAM):c.556-14A>G	rs376155665	0.00003
NC_000002.12:g.47383704_47388612del
NR_030286.1(MIR559):n.278_23134del

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