PAFAH1B2 c.81+1237T>A

Variant ID: 11-117024481-T-A

NM_002572.3(PAFAH1B2):c.81+1237T>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.

Plos One
Wood, Andrew R AR; Perry, John R B JR; Tanaka, Toshiko T; Hernandez, Dena G DG; Zheng, Hou-Feng HF; Melzer, David D; Gibbs, J Raphael JR; Nalls, Michael A MA; Weedon, Michael N MN; Spector, Tim D TD; Richards, J Brent JB; Bandinelli, Stefania S; Ferrucci, Luigi L; Singleton, Andrew B AB; Frayling, Timothy M TM
Publication Date: 2013

Variant appearance in text: rs7940310
PubMed Link: 23696881
Variant Present in the following documents:
  • Main text
  • pone.0064343.pdf
View BVdb publication page