RNF130 c.693+7965C>T

Variant ID: 5-179432096-G-A

NM_018434.5(RNF130):c.693+7965C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Association of genetic polymorphisms of PCSK9 with type 2 diabetes in Uygur Chinese population.

Bmc Cardiovascular Disorders
Wang, Meng-Meng MM; Lu, Chen-Fei CF; Yan, Shi-Qi SQ; Wang, Bao-Zhu BZ; Yesitayi, Gulinazi G; Tian, Yong-Liang YL; Xiang-Ma, ; Ma, Yi-Tong YT
Publication Date: 2022-06-22

Variant appearance in text: rs248320
PubMed Link: 35733117
Variant Present in the following documents:
  • Main text
  • 12872_2022_Article_2710.pdf
View BVdb publication page