ABCA1 c.6218C>T ;(p.T2073I)

Variant ID: 9-107549244-G-A

NM_005502.3(ABCA1):c.6218C>T;(p.T2073I)

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: 6218C>T; T2073I
PubMed Link: 30333156
Variant Present in the following documents:
  • Main text
View BVdb publication page