SEPT9 c.721+24413C>T

Variant ID: 17-75423198-C-T

NM_001113491.1(SEPT9):c.721+24413C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Allele Frequencies of the Single Nucleotide Polymorphisms Related to the Body Burden of Heavy Metals in the Korean Population and Their Ethnic Differences.

Toxicological Research
Eom, Sang-Yong SY; Lim, Ji-Ae JA; Kim, Yong-Dae YD; Choi, Byung-Sun BS; Hwang, Myung Sil MS; Park, Jung-Duck JD; Kim, Heon H; Kwon, Ho-Jang HJ
Publication Date: 2016-07

Variant appearance in text: rs312893
PubMed Link: 27437086
Variant Present in the following documents:
  • Main text
  • tr-32-195.pdf
View BVdb publication page