ANKDD1B c.601-1076G>A

Variant ID: 5-74929647-G-A

NM_001276713.1(ANKDD1B):c.601-1076G>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


BTOB: Extending the Biased GWAS to Bivariate GWAS.

Frontiers In Genetics
Zhu, Junxian J; Fan, Qiao Q; Deng, Wenying W; Wang, Yimeng Y; Guo, Xiaobo X
Publication Date: 2021

Variant appearance in text: rs253393
PubMed Link: 34025719
Variant Present in the following documents:
  • Main text
  • fgene-12-654821.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: rs253393
PubMed Link: 28438747
Variant Present in the following documents:
  • benm033277.ww1.pdf
View BVdb publication page