PCNX1 c.3868-4249G>C

Variant ID: 14-71507601-G-C

NM_014982.2(PCNX1):c.3868-4249G>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.

Annals Of Human Genetics
Cummings, Anna C AC; Jiang, Lan L; Velez Edwards, Digna R DR; McCauley, Jacob L JL; Laux, Renee R; McFarland, Lynne L LL; Fuzzell, Denise D; Knebusch, Clare C; Caywood, Laura L; Reinhart-Mercer, Lori L; Nations, Laura L; Gilbert, John R JR; Konidari, Ioanna I; Tramontana, Michael M; Cuccaro, Michael L ML; Scott, William K WK; Pericak-Vance, Margaret A MA; Haines, Jonathan L JL
Publication Date: 2012-09

Variant appearance in text: rs11848070
PubMed Link: 22881374
Variant Present in the following documents:
  • Main text
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