Genetic testing was required after the first colonoscopy and they checked, I dunno, 180? 200? known gene markers for cancer?

I was clean on all of them, but they turned up one abnormality that is flagged as “unknown” for cancer risk:

"FLCN Variant, Unknown Significance: p.G66E

Variant of Unknown Significance Detected"

I can’t remember what all that means, but it’s a crazy small variant. One section of one gene, they found a “E” where they expected a “G”.

“Wait, ‘E’? I saw GATTACA - ‘E’ isn’t DNA!”

Correct!