ABCA1 c.1529T>G ;(p.L510R)

Variant ID: 9-107594089-A-C

NM_005502.3(ABCA1):c.1529T>G;(p.L510R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic and secondary causes of severe HDL deficiency and cardiovascular disease.

Journal Of Lipid Research
Geller, Andrew S AS; Polisecki, Eliana Y EY; Diffenderfer, Margaret R MR; Asztalos, Bela F BF; Karathanasis, Sotirios K SK; Hegele, Robert A RA; Schaefer, Ernst J EJ
Publication Date: 2018-12

Variant appearance in text: ABCA1: 1529T>G; L510R
PubMed Link: 30333156
Variant Present in the following documents:
  • Main text
View BVdb publication page