HMGA2 c.250-6961G>T

Variant ID: 12-66338202-G-T

NM_003483.4(HMGA2):c.250-6961G>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Phenotype-genotype correlations of facial width and height proportions in patients with Class II malocclusion.

Orthodontics & Craniofacial Research
Moreno Uribe, L M LM; Ray, A A; Blanchette, D R DR; Dawson, D V DV; Southard, T E TE
Publication Date: 2015-04

Variant appearance in text: rs17101923
PubMed Link: 25865538
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.

Human Molecular Genetics
Fatemifar, Ghazaleh G; Hoggart, Clive J CJ; Paternoster, Lavinia L; Kemp, John P JP; Prokopenko, Inga I; Horikoshi, Momoko M; Wright, Victoria J VJ; Tobias, Jon H JH; Richmond, Stephen S; Zhurov, Alexei I AI; Toma, Arshed M AM; Pouta, Anneli A; Taanila, Anja A; Sipila, Kirsi K; Lähdesmäki, Raija R; Pillas, Demetris D; Geller, Frank F; Feenstra, Bjarke B; Melbye, Mads M; Nohr, Ellen A EA; Ring, Susan M SM; St Pourcain, Beate B; Timpson, Nicholas J NJ; Davey Smith, George G; Jarvelin, Marjo-Riitta MR; Evans, David M DM
Publication Date: 2013-09-15

Variant appearance in text: rs17101923
PubMed Link: 23704328
Variant Present in the following documents:
  • Main text
  • ddt231.pdf
View BVdb publication page