Editing Penetrance (section)

=== Complete penetrance ===
If 100% of individuals carrying a particular genotype express the associated trait, the genotype is said to show complete penetrance.<ref name=":0" /> [[neurofibromatosis type 1|Neurofibromatosis type 1 (NF1)]], is an autosomal dominant condition which shows complete penetrance, consequently everyone who inherits the disease-causing variant of this gene will develop some degree of symptoms for NF1.<ref name=":2">{{Cite journal |last1=Pacot |first1=Laurence |last2=Pelletier |first2=Valerie |last3=Chansavang |first3=Albain |last4=Briand-Suleau |first4=Audrey |last5=Burin des Roziers |first5=Cyril |last6=Coustier |first6=Audrey |last7=Maillard |first7=Theodora |last8=Vaucouleur |first8=Nicolas |last9=Orhant |first9=Lucie |last10=Barbance |first10=Cécile |last11=Lermine |first11=Alban |last12=Hamzaoui |first12=Nadim |last13=Hadjadj |first13=Djihad |last14=Laurendeau |first14=Ingrid |last15=El Khattabi |first15=Laïla |date=1 January 2023 |title=Contribution of whole genome sequencing in the molecular diagnosis of mosaic partial deletion of the NF1 gene in neurofibromatosis type 1 |url=https://doi.org/10.1007/s00439-022-02476-3 |journal=Human Genetics |language=en |volume=142 |issue=1 |pages=1–9 |doi=10.1007/s00439-022-02476-3 |pmid=35941319 |s2cid=251445081 |issn=1432-1203 |url-access=subscription }}</ref>