PCDH11X c.3034-24989C>T

Variant ID: X-91431385-C-T

NM_032968.3(PCDH11X):c.3034-24989C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs5941047
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
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: rs5941047
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: rs5941047
PubMed Link: 19136949
Variant Present in the following documents:
  • Main text
View BVdb publication page