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rs786204882

From SNPedia

ClinVar
Risk rs786204882(;)
Alt rs786204882(;)
Reference rs786204882(AGATCGTTAGCAGAAAC;AGATCGTTAGCAGAAAC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN LOC101929706 KLLN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89624247_89624263del17
CLNSRC
CLNACC RCV000169823.1,