ABCG8 c.1795_1796delinsAC ;(p.C599T)

Variant ID: 2-44104738-TG-AC

NM_022437.2(ABCG8):c.1795_1796delinsAC;(p.C599T)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetics of coronary artery disease and myocardial infarction.

World Journal Of Cardiology
Dai, Xuming X; Wiernek, Szymon S; Evans, James P JP; Runge, Marschall S MS
Publication Date: 2016-01-26

Variant appearance in text: ABCG8: C599T
PubMed Link: 26839654
Variant Present in the following documents:
  • Main text
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