DNM2 c.1672-3556G>C

Variant ID: 19-10927100-G-C

NM_001005361.2(DNM2):c.1672-3556G>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Multi-Omics Analysis Reveals MicroRNAs Associated With Cardiometabolic Traits.

Frontiers In Genetics
Mens, Michelle M J MMJ; Maas, Silvana C E SCE; Klap, Jaco J; Weverling, Gerrit Jan GJ; Klatser, Paul P; Brakenhoff, Just P J JPJ; van Meurs, Joyce B J JBJ; Uitterlinden, André G AG; Ikram, M Arfan MA; Kavousi, Maryam M; Ghanbari, Mohsen M
Publication Date: 2020

Variant appearance in text: rs3786719
PubMed Link: 32174972
Variant Present in the following documents:
  • Main text
  • fgene-11-00110.pdf
View BVdb publication page



Low LDL cholesterol, PCSK9 and HMGCR genetic variation, and risk of Alzheimer's disease and Parkinson's disease: Mendelian randomisation study.

Bmj (Clinical Research Ed.)
Benn, Marianne M; Nordestgaard, Børge G BG; Frikke-Schmidt, Ruth R; Tybjærg-Hansen, Anne A
Publication Date: 2017-04-24

Variant appearance in text: rs3786719
PubMed Link: 28438747
Variant Present in the following documents:
  • benm033277.ww1.pdf
View BVdb publication page