PCDH11X c.3115-21526A>G

Variant ID: X-91496587-A-G

NM_032968.3(PCDH11X):c.3115-21526A>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


The possible role of chromosome X variability in hypertensive familiarity.

Journal Of Human Hypertension
Ciccarelli, M M; Finelli, R R; Rivera, N N; Santulli, G G; Izzo, R R; De Luca, N N; Rozza, F F; Ceccarelli, M M; Pagnotta, S S; Uliano, F F; Tremigliozzi, R R; Condorelli, G G; Trimarco, V V; Iaccarino, G G
Publication Date: 2017-01

Variant appearance in text: rs117393
PubMed Link: 26911533
Variant Present in the following documents:
  • jhh20169a.pdf
View BVdb publication page



PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility.

Psychiatric Genetics
Beecham, Gary W GW; Naj, Adam C AC; Gilbert, John R JR; Haines, Jonathan L JL; Buxbaum, Joseph D JD; Pericak-Vance, Margaret A MA
Publication Date: 2010-12

Variant appearance in text: rs117393
PubMed Link: 20523261
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease.

Nature Genetics
Carrasquillo, Minerva M MM; Zou, Fanggeng F; Pankratz, V Shane VS; Wilcox, Samantha L SL; Ma, Li L; Walker, Louise P LP; Younkin, Samuel G SG; Younkin, Curtis S CS; Younkin, Linda H LH; Bisceglio, Gina D GD; Ertekin-Taner, Nilufer N; Crook, Julia E JE; Dickson, Dennis W DW; Petersen, Ronald C RC; Graff-Radford, Neill R NR; Younkin, Steven G SG
Publication Date: 2009-02

Variant appearance in text: rs117393
PubMed Link: 19136949
Variant Present in the following documents:
  • Main text
View BVdb publication page