PCSK2 c.283-26899A>T

Variant ID: 20-17312073-A-T

NM_002594.3(PCSK2):c.283-26899A>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Linkage analysis of plasma dopamine β-hydroxylase activity in families of patients with schizophrenia.

Human Genetics
Cubells, Joseph F JF; Sun, Xiangqing X; Li, Wenbiao W; Bonsall, Robert W RW; McGrath, John A JA; Avramopoulos, Dimitri D; Lasseter, Virginia K VK; Wolyniec, Paula S PS; Tang, Yi-Lang YL; Mercer, Kristina K; Pulver, Ann E AE; Elston, Robert C RC
Publication Date: 2011-11

Variant appearance in text: rs727472
PubMed Link: 21509519
Variant Present in the following documents:
  • Main text
View BVdb publication page



A genome-wide scan for genes involved in primary vesicoureteric reflux.

Journal Of Medical Genetics
Kelly, H H; Molony, C M CM; Darlow, J M JM; Pirker, M E ME; Yoneda, A A; Green, A J AJ; Puri, P P; Barton, D E DE
Publication Date: 2007-11

Variant appearance in text: rs727472
PubMed Link: 17660461
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of the proprotein convertase subtilisin/kexin-type 2 (PCSK2) gene with type 2 diabetes in an African American population.

Molecular Genetics And Metabolism
Leak, Tennille S TS; Keene, Keith L KL; Langefeld, Carl D CD; Gallagher, Carla J CJ; Mychaleckyj, Josyf C JC; Freedman, Barry I BI; Bowden, Donald W DW; Rich, Stephen S SS; Sale, Michèle M MM
Publication Date: 2007

Variant appearance in text: rs727472
PubMed Link: 17618154
Variant Present in the following documents:
  • Main text
View BVdb publication page