ACVR2A c.55+16970T>C

Variant ID: 2-148619746-T-C

NM_001616.4(ACVR2A):c.55+16970T>C

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Family-based analysis of candidate genes for polycystic ovary syndrome.

The Journal Of Clinical Endocrinology And Metabolism
Ewens, Kathryn G KG; Stewart, Douglas R DR; Ankener, Wendy W; Urbanek, Margrit M; McAllister, Jan M JM; Chen, Chen C; Baig, K Maravet KM; Parker, Stephen C J SC; Margulies, Elliot H EH; Legro, Richard S RS; Dunaif, Andrea A; Strauss, Jerome F JF; Spielman, Richard S RS
Publication Date: 2010-05

Variant appearance in text: rs1895694
PubMed Link: 20200332
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic association of the activin A receptor gene (ACVR2A) and pre-eclampsia.

Molecular Human Reproduction
Fitzpatrick, E E; Johnson, M P MP; Dyer, T D TD; Forrest, S S; Elliott, K K; Blangero, J J; Brennecke, S P SP; Moses, E K EK
Publication Date: 2009-03

Variant appearance in text: rs1895694
PubMed Link: 19126782
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study).

European Journal Of Human Genetics : Ejhg
Roten, Linda T LT; Johnson, Matthew P MP; Forsmo, Siri S; Fitzpatrick, Elizabeth E; Dyer, Thomas D TD; Brennecke, Shaun P SP; Blangero, John J; Moses, Eric K EK; Austgulen, Rigmor R
Publication Date: 2009-02

Variant appearance in text: rs1895694
PubMed Link: 18781190
Variant Present in the following documents:
  • Main text
View BVdb publication page



Detection of chromosomal structural alterations in single cells by SNP arrays: a systematic survey of amplification bias and optimized workflow.

Plos One
Iwamoto, Kazuya K; Bundo, Miki M; Ueda, Junko J; Nakano, Yoko Y; Ukai, Wataru W; Hashimoto, Eri E; Saito, Toshikazu T; Kato, Tadafumi T
Publication Date: 2007-12-12

Variant appearance in text: rs1895694
PubMed Link: 18074030
Variant Present in the following documents:
  • Main text
  • pone.0001306.pdf
View BVdb publication page