TNFRSF1A c.39+1732C>A

Variant ID: 12-6449210-G-T

NM_001065.3(TNFRSF1A):c.39+1732C>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


A population-based case-control study of genetic variation in cytokine genes associated with risk of cervical and vulvar cancers.

Gynecologic Oncology
Hardikar, Sheetal S; Johnson, Lisa G LG; Malkki, Mari M; Petersdorf, Effie W EW; Galloway, Denise A DA; Schwartz, Stephen M SM; Madeleine, Margaret M MM
Publication Date: 2015-10

Variant appearance in text: rs4149575
PubMed Link: 26241630
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variation in TLR or NFkappaB pathways and the risk of breast cancer: a case-control study.

Bmc Cancer
Resler, Alexa J AJ; Malone, Kathleen E KE; Johnson, Lisa G LG; Malkki, Mari M; Petersdorf, Effie W EW; McKnight, Barbara B; Madeleine, Margaret M MM
Publication Date: 2013-05-01

Variant appearance in text: rs4149575
PubMed Link: 23634849
Variant Present in the following documents:
View BVdb publication page