APOB c.875C>G ;(p.P292R)

Variant ID: 2-21257717-G-C

NM_000384.2(APOB):c.875C>G;(p.P292R)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Global genetic diversity of human apolipoproteins and effects on cardiovascular disease risk.

Journal Of Lipid Research
Zhou, Yitian Y; Mägi, Reedik R; Milani, Lili L; Lauschke, Volker M VM
Publication Date: 2018-10

Variant appearance in text: rs755277795
PubMed Link: 30076208
Variant Present in the following documents:
  • 10.1194_P086710_jlr.P086710-4.xlsx, sheet 1
View BVdb publication page



SLC7A14 linked to autosomal recessive retinitis pigmentosa.

Nature Communications
Jin, Zi-Bing ZB; Huang, Xiu-Feng XF; Lv, Ji-Neng JN; Xiang, Lue L; Li, Dong-Qing DQ; Chen, Jiangfei J; Huang, Changjiang C; Wu, Jinyu J; Lu, Fan F; Qu, Jia J
Publication Date: 2014-03-27

Variant appearance in text: APOB: P292R
PubMed Link: 24670872
Variant Present in the following documents:
  • Main text
  • ncomms4517-s1.pdf
  • ncomms4517.pdf
View BVdb publication page