LPCAT2 c.1315-744G>A

Variant ID: 16-55612277-G-A

NM_017839.4(LPCAT2):c.1315-744G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association.

Human Molecular Genetics
Wood, Andrew R AR; Hernandez, Dena G DG; Nalls, Michael A MA; Yaghootkar, Hanieh H; Gibbs, J Raphael JR; Harries, Lorna W LW; Chong, Sean S; Moore, Matthew M; Weedon, Michael N MN; Guralnik, Jack M JM; Bandinelli, Stefania S; Murray, Anna A; Ferrucci, Luigi L; Singleton, Andrew B AB; Melzer, David D; Frayling, Timothy M TM
Publication Date: 2011-10-15

Variant appearance in text: rs883180
PubMed Link: 21798870
Variant Present in the following documents:
  • Main text
  • ddr328.pdf
View BVdb publication page