F2 c.894G>T ;(p.E298D)

Variant ID: 11-46748067-G-T

NM_000506.3(F2):c.894G>T;(p.E298D)

This variant was identified in 16 publications

View GRCh38 version.




Publications:


Speed and power-related gene polymorphisms associated with playing position in elite soccer players.

Biology Of Sport
Petr, Miroslav M; Thiel, Dan D; Kateřina, Kvapilová K; Brož, Petr P; Malý, Tomáš T; Zahálka, František F; Vostatková, Pavlína P; Wilk, Michal M; Chycki, Jakub J; Stastny, Petr P
Publication Date: 2022-03

Variant appearance in text: F2: Glu298Asp
PubMed Link: 35309536
Variant Present in the following documents:
  • JBS-39-105333.pdf
View BVdb publication page



Preeclampsia, Natural History, Genes, and miRNAs Associated with the Syndrome.

Journal Of Pregnancy
Parada-Niño, Laura L; Castillo-León, Luisa Fernanda LF; Morel, Adrien A
Publication Date: 2022

Variant appearance in text: F2: Glu298Asp
PubMed Link: 35198246
Variant Present in the following documents:
  • JP2022-3851225.pdf
View BVdb publication page



Association of NOS3 (rs 2070744) and SOD2Val16Ala (rs4880) gene polymorphisms with increased risk of ESRD among Egyptian patients.

Journal, Genetic Engineering & Biotechnology
Elsaid, Afaf A; Samir Eid, Omnia O; Said, Samy B SB; Zahran, Rasha F RF
Publication Date: 2021-10-18

Variant appearance in text: F2: Glu298Asp
PubMed Link: 34661767
Variant Present in the following documents:
  • Main text
  • 43141_2021_Article_260.pdf
View BVdb publication page



Heritability for stroke: Essential for taking family history.

Caspian Journal Of Internal Medicine
Pourasgari, Masoumeh M; Mohamadkhani, Ashraf A
Publication Date: 2020-05

Variant appearance in text: F2: E298D
PubMed Link: 32874429
Variant Present in the following documents:
  • Main text
  • cjim-11-237.pdf
View BVdb publication page



Designing and Validation of One-Step T-ARMS-PCR for Genotyping the eNOS rs1799983 SNP.

Iranian Journal Of Biotechnology
Heidar, Mohammad Mehdi MM; Khatami, Mehri M
Publication Date: 2017

Variant appearance in text: F2: Glu298Asp
PubMed Link: 29845071
Variant Present in the following documents:
  • Main text
View BVdb publication page



Population-based Study of Risk Polymorphisms Associated with Vascular Disorders and Dementia.

Current Genomics
Teijido, Óscar Ó; Carril, Juan Carlos JC; Cacabelos, Ramón R
Publication Date: 2017-10

Variant appearance in text: F2: Glu298Asp
PubMed Link: 29081698
Variant Present in the following documents:
  • Main text
View BVdb publication page



Endometriosis and headache.

Current Pain And Headache Reports
Stovner, Lars Jacob LJ; Aegidius, Karen K; Linde, Mattias M
Publication Date: 2011-10

Variant appearance in text: F2: Glu298Asp
PubMed Link: 21556708
Variant Present in the following documents:
  • 11916_2011_Article_209.pdf
View BVdb publication page



The genetics of pre-eclampsia and other hypertensive disorders of pregnancy.

Best Practice & Research. Clinical Obstetrics & Gynaecology
Williams, Paula J PJ; Broughton Pipkin, Fiona F
Publication Date: 2011-08

Variant appearance in text: F2: E298D
PubMed Link: 21429808
Variant Present in the following documents:
  • Main text
View BVdb publication page



Novel pathway analysis of genomic polymorphism-cancer risk interaction in the Breast Cancer Prevention Trial.

International Journal Of Molecular Epidemiology And Genetics
Dunn, Barbara K BK; Greene, Mark H MH; Kelley, Jenny M JM; Costantino, Joseph P JP; Clifford, Robert J RJ; Hu, Ying Y; Tang, Gong G; Kazerouni, Neely N; Rosenberg, Philip S PS; Meerzaman, Daoud M DM; Buetow, Kenneth H KH
Publication Date: 2010

Variant appearance in text: F2: Glu298Asp
PubMed Link: 21152245
Variant Present in the following documents:
  • Main text
View BVdb publication page



Lack of replication in polymorphisms reported to be associated with atrial fibrillation.

Heart Rhythm
Sinner, Moritz F MF; Lubitz, Steven A SA; Pfeufer, Arne A; Makino, Seiko S; Beckmann, Britt-Maria BM; Lunetta, Kathryn L KL; Steinbeck, Gerhard G; Perz, Siegfried S; Rahman, Rosanna R; Sonni, Akshata A; Greenberg, Steven M SM; Furie, Karen L KL; Wichmann, H-Erich HE; Meitinger, Thomas T; Peters, Annette A; Benjamin, Emelia J EJ; Rosand, Jonathan J; Ellinor, Patrick T PT; Kääb, Stefan S
Publication Date: 2011-03

Variant appearance in text: F2: E298D
PubMed Link: 21056700
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of fetal inflammation and coagulation pathway gene polymorphisms with neurodevelopmental delay at age 2 years.

American Journal Of Obstetrics And Gynecology
Clark, Erin A S EA; Mele, Lisa L; Wapner, Ronald J RJ; Spong, Catherine Y CY; Sorokin, Yoram Y; Peaceman, Alan A; Iams, Jay D JD; Leveno, Kenneth J KJ; Harper, Margaret M; Caritis, Steve N SN; Miodovnik, Menachem M; Mercer, Brian M BM; Thorp, John M JM; Ramin, Susan M SM; Carpenter, Marshall M; Rouse, Dwight J DJ; ,
Publication Date: 2010-07

Variant appearance in text: F2: glu298asp
PubMed Link: 20417488
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of congenital cardiovascular malformations with 33 single nucleotide polymorphisms of selected cardiovascular disease-related genes.

Birth Defects Research. Part A, Clinical And Molecular Teratology
Kuehl, Karen K; Loffredo, Christopher C; Lammer, Edward J EJ; Iovannisci, David M DM; Shaw, Gary M GM
Publication Date: 2010-02

Variant appearance in text: F2: Glu298Asp
PubMed Link: 19764075
Variant Present in the following documents:
  • Main text
View BVdb publication page



Candidate gene polymorphisms for ischemic stroke.

Stroke
Matarin, Mar M; Brown, W Mark WM; Dena, Hernandez H; Britton, Angela A; De Vrieze, Fabienne Wavrant FW; Brott, Thomas G TG; Brown, Robert D RD; Worrall, Bradford B BB; Case, L Douglas LD; Chanock, Stephen J SJ; Metter, E Jeffrey EJ; Ferruci, Luigi L; Gamble, Dale D; Hardy, John A JA; Rich, Stephen S SS; Singleton, Andrew A; Meschia, James F JF
Publication Date: 2009-11

Variant appearance in text: F2: glu298asp
PubMed Link: 19729601
Variant Present in the following documents:
  • Main text
View BVdb publication page



Prevalence in the United States of selected candidate gene variants: Third National Health and Nutrition Examination Survey, 1991-1994.

American Journal Of Epidemiology
Chang, Man-Huei MH; Lindegren, Mary Lou ML; Butler, Mary A MA; Chanock, Stephen J SJ; Dowling, Nicole F NF; Gallagher, Margaret M; Moonesinghe, Ramal R; Moore, Cynthia A CA; Ned, Renée M RM; Reichler, Mary R MR; Sanders, Christopher L CL; Welch, Robert R; Yesupriya, Ajay A; Khoury, Muin J MJ; ,
Publication Date: 2009-01-01

Variant appearance in text: F2: E298D
PubMed Link: 18936436
Variant Present in the following documents:
  • Main text
View BVdb publication page



Immunology and genetic of preeclampsia.

Clinical & Developmental Immunology
Serrano, Norma C NC
Publication Date: 2006

Variant appearance in text: F2: Glu298Asp
PubMed Link: 17162362
Variant Present in the following documents:
  • CDI-13-197.pdf
View BVdb publication page



Quantitative analysis of SMN1 gene and estimation of SMN1 deletion carrier frequency in Korean population based on real-time PCR.

Journal Of Korean Medical Science
Lee, Tae-Mi TM; Kim, Sang-Wun SW; Lee, Kwang-Soo KS; Jin, Hyun-Seok HS; Koo, Soo Kyung SK; Jo, Inho I; Kang, Seongman S; Jung, Sung-Chul SC
Publication Date: 2004-12

Variant appearance in text: F2: Glu298Asp
PubMed Link: 15608400
Variant Present in the following documents:
  • jkms-19-870.pdf
View BVdb publication page