CYP19A1 c.-39+6907T>C

Variant ID: 15-51623785-A-G

NM_000103.4(CYP19A1):c.-39+6907T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


CYP19A1 single nucleotide polymorphism associations with CYP19A1, NFκB1, and IL6 gene expression in human normal colon and normal liver samples.

Pharmacogenomics And Personalized Medicine
Penney, Rosalind B RB; Lundgreen, Abbie A; Yao-Borengasser, Aiwei A; Edavana, Vineetha K VK; Williams, Suzanne S; Dhakal, Ishwori I; Wolff, Roger K RK; Kadlubar, Susan S; Slattery, Martha L ML
Publication Date: 2014

Variant appearance in text: rs8025191
PubMed Link: 25114581
Variant Present in the following documents:
  • Main text
  • pgpm-7-163.pdf
View BVdb publication page



Associations between CYP19A1 polymorphisms, Native American ancestry, and breast cancer risk and mortality: the Breast Cancer Health Disparities Study.

Cancer Causes & Control : Ccc
Boone, Stephanie D SD; Baumgartner, Kathy B KB; Baumgartner, Richard N RN; Connor, Avonne E AE; Pinkston, Christina M CM; Rai, Shesh N SN; Riley, Elizabeth C EC; Hines, Lisa M LM; Giuliano, Anna R AR; John, Esther M EM; Stern, Mariana C MC; Torres-Mejía, Gabriela G; Wolff, Roger K RK; Slattery, Martha L ML
Publication Date: 2014-11

Variant appearance in text: rs8025191
PubMed Link: 25088806
Variant Present in the following documents:
  • Main text
View BVdb publication page