ClinVar Miner

List of variants reported as pathogenic for secretory diarrhea by Institute of Human Genetics, University of Leipzig Medical Center

Included ClinVar conditions (8):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_002354.3(EPCAM):c.556-14A>G	rs376155665	0.00003
NM_001080467.3(MYO5B):c.4090C>T (p.Gln1364Ter)	rs1264355256

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