CSMD1 c.302+56806A>C

Variant ID: 8-4438058-T-G

NM_033225.5(CSMD1):c.302+56806A>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease.

Nature Neuroscience
Huang, Kuan-Lin KL; Marcora, Edoardo E; Pimenova, Anna A AA; Di Narzo, Antonio F AF; Kapoor, Manav M; Jin, Sheng Chih SC; Harari, Oscar O; Bertelsen, Sarah S; Fairfax, Benjamin P BP; Czajkowski, Jake J; Chouraki, Vincent V; Grenier-Boley, Benjamin B; Bellenguez, Céline C; Deming, Yuetiva Y; McKenzie, Andrew A; Raj, Towfique T; Renton, Alan E AE; Budde, John J; Smith, Albert A; Fitzpatrick, Annette A; Bis, Joshua C JC; DeStefano, Anita A; Adams, Hieab H H HHH; Ikram, M Arfan MA; van der Lee, Sven S; Del-Aguila, Jorge L JL; Fernandez, Maria Victoria MV; Ibañez, Laura L; , ; , ; Sims, Rebecca R; Escott-Price, Valentina V; Mayeux, Richard R; Haines, Jonathan L JL; Farrer, Lindsay A LA; Pericak-Vance, Margaret A MA; Lambert, Jean Charles JC; van Duijn, Cornelia C; Launer, Lenore L; Seshadri, Sudha S; Williams, Julie J; Amouyel, Philippe P; Schellenberg, Gerard D GD; Zhang, Bin B; Borecki, Ingrid I; Kauwe, John S K JSK; Cruchaga, Carlos C; Hao, Ke K; Goate, Alison M AM
Publication Date: 2017-08

Variant appearance in text: rs2725066
PubMed Link: 28628103
Variant Present in the following documents:
  • Main text
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