SLC9A9 c.378+5099C>T

Variant ID: 3-143545762-G-A

NM_173653.3(SLC9A9):c.378+5099C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Construction of gene clusters resembling genetic causal mechanisms for common complex disease with an application to young-onset hypertension.

Bmc Genomics
Lynn, Ke-Shiuan KS; Lu, Chen-Hua CH; Yang, Han-Ying HY; Hsu, Wen-Lian WL; Pan, Wen-Harn WH
Publication Date: 2013-07-23

Variant appearance in text: rs16854417
PubMed Link: 23879630
Variant Present in the following documents:
  • Main text
  • 1471-2164-14-497.pdf
View BVdb publication page