PPARG c.-8-1728T>C

Variant ID: 3-12419475-T-C

NM_138711.6(PPARG):c.-8-1728T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Metabolic heritability at birth: implications for chronic disease research.

Human Genetics
Ryckman, Kelli K KK; Smith, Caitlin J CJ; Jelliffe-Pawlowski, Laura L LL; Momany, Allison M AM; Berberich, Stanton L SL; Murray, Jeffrey C JC
Publication Date: 2014-08

Variant appearance in text: rs2921190
PubMed Link: 24850141
Variant Present in the following documents:
  • Main text
View BVdb publication page