PDE3B c.2321-3856T>G

Variant ID: 11-14861517-T-G

NM_000922.3(PDE3B):c.2321-3856T>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic variation in GC and CYP2R1 affects 25-hydroxyvitamin D concentration and skeletal parameters: A genome-wide association study in 24-month-old Finnish children.

Plos Genetics
Kämpe, Anders A; Enlund-Cerullo, Maria M; Valkama, Saara S; Holmlund-Suila, Elisa E; Rosendahl, Jenni J; Hauta-Alus, Helena H; Pekkinen, Minna M; Andersson, Sture S; Mäkitie, Outi O
Publication Date: 2019-12

Variant appearance in text: rs11023350
PubMed Link: 31841498
Variant Present in the following documents:
  • Main text
  • pgen.1008530.pdf
View BVdb publication page



Vitamin D and cognitive function: A Mendelian randomisation study.

Scientific Reports
Maddock, Jane J; Zhou, Ang A; Cavadino, Alana A; Kuźma, Elżbieta E; Bao, Yanchun Y; Smart, Melissa C MC; Saum, Kai-Uwe KU; Schöttker, Ben B; Engmann, Jorgen J; Kjærgaard, Marie M; Karhunen, Ville V; Zhan, Yiqiang Y; Lehtimäki, Terho T; Rovio, Suvi P SP; Byberg, Liisa L; Lahti, Jari J; Marques-Vidal, Pedro P; Sen, Abhijit A; Perna, Laura L; Schirmer, Henrik H; Singh-Manoux, Archana A; Auvinen, Juha J; Hutri-Kähönen, Nina N; Kähönen, Mika M; Kilander, Lena L; Räikkönen, Katri K; Melhus, Håkan H; Ingelsson, Erik E; Guessous, Idris I; Petrovic, Katja E KE; Schmidt, Helena H; Schmidt, Reinhold R; Vollenweider, Peter P; Lind, Lars L; Eriksson, Johan G JG; Michaëlsson, Karl K; Raitakari, Olli T OT; Hägg, Sara S; Pedersen, Nancy L NL; Herzig, Karl-Heinz KH; Järvelin, Marjo-Riitta MR; Veijola, Juha J; Kivimaki, Mika M; Jorde, Rolf R; Brenner, Hermann H; Kumari, Meena M; Power, Chris C; Llewellyn, David J DJ; Hyppönen, Elina E
Publication Date: 2017-10-16

Variant appearance in text: rs11023350
PubMed Link: 29038561
Variant Present in the following documents:
  • 41598_2017_13189_MOESM1_ESM.pdf
View BVdb publication page