LDLR c.1977C>G ;(p.T659=)

Variant ID: 19-11230899-C-G

NM_000527.4(LDLR):c.1977C>G;(p.T659=)

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: LDLR: T659T
PubMed Link: 30333156
Variant Present in the following documents:
  • Main text
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