ClinVar Miner

List of variants reported as likely pathogenic for colorectal cancer by Genetica Molecular, Fundacion para el Progreso de la Medicina

Included ClinVar conditions (91):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_002354.3(EPCAM):c.904-1_904del rs2103770769

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