PGR c.1789+11724G>A

Variant ID: 11-100985014-C-T

NM_000926.4(PGR):c.1789+11724G>A

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Variant Alleles of the ESR1, PPARG, HMGA2, and MTHFR Genes Are Associated With Polycystic Ovary Syndrome Risk in a Chinese Population: A Case-Control Study.

Frontiers In Endocrinology
Jiao, Xianting X; Chen, Weiwei W; Zhang, Jun J; Wang, Weiye W; Song, Junjiao J; Chen, Dan D; Zhu, Wenting W; Shi, Yuhua Y; Yu, Xiaodan X
Publication Date: 2018

Variant appearance in text: rs566351
PubMed Link: 30214429
Variant Present in the following documents:
  • Main text
  • fendo-09-00504.pdf
View BVdb publication page



Association of progesterone receptor gene (PGR) variants and breast cancer risk in African American women.

Breast Cancer Research And Treatment
Gabriel, Courtney A CA; Mitra, Nandita N; Demichele, Angela A; Rebbeck, Timothy T
Publication Date: 2013-06

Variant appearance in text: rs566351
PubMed Link: 23764995
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic susceptibility factors on genes involved in the steroid hormone biosynthesis pathway and progesterone receptor for gastric cancer risk.

Plos One
Cho, Lisa Y LY; Yang, Jae Jeong JJ; Ko, Kwang-Pil KP; Ma, Seung Hyun SH; Shin, Aesun A; Choi, Bo Youl BY; Han, Dong Soo DS; Song, Kyu Sang KS; Kim, Yong Sung YS; Chang, Soung-Hoon SH; Shin, Hai-Rim HR; Kang, Daehee D; Yoo, Keun-Young KY; Park, Sue K SK
Publication Date: 2012

Variant appearance in text: rs566351
PubMed Link: 23110082
Variant Present in the following documents:
  • Main text
  • pone.0047603.pdf
View BVdb publication page



An improved PSO algorithm for generating protective SNP barcodes in breast cancer.

Plos One
Chuang, Li-Yeh LY; Lin, Yu-Da YD; Chang, Hsueh-Wei HW; Yang, Cheng-Hong CH
Publication Date: 2012

Variant appearance in text: rs566351
PubMed Link: 22623973
Variant Present in the following documents:
  • Main text
  • pone.0037018.pdf
View BVdb publication page



Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.

American Journal Of Human Genetics
Suarez, Brian K BK; Duan, Jubao J; Sanders, Alan R AR; Hinrichs, Anthony L AL; Jin, Carol H CH; Hou, Cuiping C; Buccola, Nancy G NG; Hale, Nancy N; Weilbaecher, Ann N AN; Nertney, Deborah A DA; Olincy, Ann A; Green, Susan S; Schaffer, Arthur W AW; Smith, Christopher J CJ; Hannah, Dominique E DE; Rice, John P JP; Cox, Nancy J NJ; Martinez, Maria M; Mowry, Bryan J BJ; Amin, Farooq F; Silverman, Jeremy M JM; Black, Donald W DW; Byerley, William F WF; Crowe, Raymond R RR; Freedman, Robert R; Cloninger, C Robert CR; Levinson, Douglas F DF; Gejman, Pablo V PV
Publication Date: 2006-02

Variant appearance in text: rs566351
PubMed Link: 16400611
Variant Present in the following documents:
  • Main text
View BVdb publication page