ANKDD1B c.396+1624A>G

Variant ID: 5-74917862-A-G

NM_001276713.1(ANKDD1B):c.396+1624A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Molecular genetic overlap between migraine and major depressive disorder.

European Journal Of Human Genetics : Ejhg
Yang, Yuanhao Y; Zhao, Huiying H; Boomsma, Dorret I DI; Ligthart, Lannie L; Belin, Andrea C AC; Smith, George Davey GD; Esko, Tonu T; Freilinger, Tobias M TM; Hansen, Thomas Folkmann TF; Ikram, M Arfan MA; Kallela, Mikko M; Kubisch, Christian C; Paraskevi, Christofidou C; Strachan, David P DP; Wessman, Maija M; , ; van den Maagdenberg, Arn M J M AMJM; Terwindt, Gisela M GM; Nyholt, Dale R DR
Publication Date: 2018-08

Variant appearance in text: rs904743
PubMed Link: 29995844
Variant Present in the following documents:
  • Main text
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: rs904743
PubMed Link: 28438747
Variant Present in the following documents:
  • benm033277.ww1.pdf
View BVdb publication page