PGR c.1789+2063C>T

Variant ID: 11-100994675-G-A

NM_000926.4(PGR):c.1789+2063C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer
Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F
Publication Date: 2017-05-12

Variant appearance in text: rs481775
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page



Genetic variation in the progesterone receptor gene and risk of endometrial cancer: a haplotype-based approach.

Carcinogenesis
Lee, Eunjung E; Hsu, Chris C; Haiman, Christopher A CA; Razavi, Pedram P; Horn-Ross, Pamela L PL; Van Den Berg, David D; Bernstein, Leslie L; Le Marchand, Loic L; Henderson, Brian E BE; Setiawan, V Wendy VW; Ursin, Giske G
Publication Date: 2010-08

Variant appearance in text: rs481775
PubMed Link: 20547493
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variation in sex-steroid receptors and synthesizing enzymes and colorectal cancer risk in women.

Cancer Causes & Control : Ccc
Lin, Jennifer J; Zee, Robert Y L RY; Liu, Kuang-Yu KY; Zhang, Shumin M SM; Lee, I-Min IM; Manson, JoAnn E JE; Giovannucci, Edward E; Buring, Julie E JE; Cook, Nancy R NR
Publication Date: 2010-06

Variant appearance in text: rs481775
PubMed Link: 20148360
Variant Present in the following documents:
  • Main text
View BVdb publication page