F7 c.506-204G>A

Variant ID: 13-113770876-G-A

NM_019616.3(F7):c.506-204G>A

This variant was identified in 11 publications

View GRCh38 version.




Publications:


Genetic predictors of severe intraventricular hemorrhage in extremely low-birthweight infants.

Journal Of Perinatology : Official Journal Of The California Perinatal Association
Thornburg, Courtney D CD; Erickson, Stephen W SW; Page, Grier P GP; Clark, Erin A S EAS; DeAngelis, Margaret M MM; Hartnett, M Elizabeth ME; Goldstein, Ricki F RF; Dagle, John M JM; Murray, Jeffrey C JC; Poindexter, Brenda B BB; Das, Abhik A; Cotten, C Michael CM; ,
Publication Date: 2021-02

Variant appearance in text: rs488703
PubMed Link: 32978526
Variant Present in the following documents:
  • Main text
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iFunMed: Integrative functional mediation analysis of GWAS and eQTL studies.

Genetic Epidemiology
Rojo, Constanza C; Zhang, Qi Q; Keleş, Sündüz S
Publication Date: 2019-10

Variant appearance in text: rs488703
PubMed Link: 31328826
Variant Present in the following documents:
  • Main text
View BVdb publication page



Associations of activated coagulation factor VII and factor VIIa-antithrombin levels with genome-wide polymorphisms and cardiovascular disease risk.

Journal Of Thrombosis And Haemostasis : Jth
Olson, N C NC; Raffield, L M LM; Lange, L A LA; Lange, E M EM; Longstreth, W T WT; Chauhan, G G; Debette, S S; Seshadri, S S; Reiner, A P AP; Tracy, R P RP
Publication Date: 2018-01

Variant appearance in text: rs488703
PubMed Link: 29112333
Variant Present in the following documents:
  • Main text
View BVdb publication page



Connecting genetic risk to disease end points through the human blood plasma proteome.

Nature Communications
Suhre, Karsten K; Arnold, Matthias M; Bhagwat, Aditya Mukund AM; Cotton, Richard J RJ; Engelke, Rudolf R; Raffler, Johannes J; Sarwath, Hina H; Thareja, Gaurav G; Wahl, Annika A; DeLisle, Robert Kirk RK; Gold, Larry L; Pezer, Marija M; Lauc, Gordan G; El-Din Selim, Mohammed A MA; Mook-Kanamori, Dennis O DO; Al-Dous, Eman K EK; Mohamoud, Yasmin A YA; Malek, Joel J; Strauch, Konstantin K; Grallert, Harald H; Peters, Annette A; Kastenmüller, Gabi G; Gieger, Christian C; Graumann, Johannes J
Publication Date: 2017-02-27

Variant appearance in text: rs488703
PubMed Link: 28240269
Variant Present in the following documents:
  • ncomms14357-s1.pdf
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Influence of genetic variation on plasma protein levels in older adults using a multi-analyte panel.

Plos One
Kim, Sungeun S; Swaminathan, Shanker S; Inlow, Mark M; Risacher, Shannon L SL; Nho, Kwangsik K; Shen, Li L; Foroud, Tatiana M TM; Petersen, Ronald C RC; Aisen, Paul S PS; Soares, Holly H; Toledo, Jon B JB; Shaw, Leslie M LM; Trojanowski, John Q JQ; Weiner, Michael W MW; McDonald, Brenna C BC; Farlow, Martin R MR; Ghetti, Bernardino B; Saykin, Andrew J AJ; ,
Publication Date: 2013

Variant appearance in text: rs488703
PubMed Link: 23894628
Variant Present in the following documents:
  • Main text
  • pone.0070269.pdf
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Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.

American Journal Of Human Genetics
Tang, Weihong W; Schwienbacher, Christine C; Lopez, Lorna M LM; Ben-Shlomo, Yoav Y; Oudot-Mellakh, Tiphaine T; Johnson, Andrew D AD; Samani, Nilesh J NJ; Basu, Saonli S; Gögele, Martin M; Davies, Gail G; Lowe, Gordon D O GD; Tregouet, David-Alexandre DA; Tan, Adrian A; Pankow, James S JS; Tenesa, Albert A; Levy, Daniel D; Volpato, Claudia B CB; Rumley, Ann A; Gow, Alan J AJ; Minelli, Cosetta C; Yarnell, John W G JW; Porteous, David J DJ; Starr, John M JM; Gallacher, John J; Boerwinkle, Eric E; Visscher, Peter M PM; Pramstaller, Peter P PP; Cushman, Mary M; Emilsson, Valur V; Plump, Andrew S AS; Matijevic, Nena N; Morange, Pierre-Emmanuel PE; Deary, Ian J IJ; Hicks, Andrew A AA; Folsom, Aaron R AR
Publication Date: 2012-07-13

Variant appearance in text: rs488703
PubMed Link: 22703881
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association between polymorphisms in the coagulation factor VII gene and coronary heart disease risk in different ethnicities: a meta-analysis.

Bmc Medical Genetics
Mo, Xingbo X; Hao, Yongchen Y; Yang, Xueli X; Chen, Shufeng S; Lu, Xiangfeng X; Gu, Dongfeng D
Publication Date: 2011-08-12

Variant appearance in text: rs488703
PubMed Link: 21838885
Variant Present in the following documents:
  • Main text
  • 1471-2350-12-107.pdf
View BVdb publication page



Novel loci involved in platelet function and platelet count identified by a genome-wide study performed in children.

Haematologica
Guerrero, José A JA; Rivera, José J; Quiroga, Teresa T; Martinez-Perez, Angel A; Antón, Ana Isabel AI; Martínez, Constantino C; Panes, Olga O; Vicente, Vicente V; Mezzano, Diego D; Soria, José-Manuel JM; Corral, Javier J
Publication Date: 2011-09

Variant appearance in text: rs488703
PubMed Link: 21546496
Variant Present in the following documents:
  • Main text
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Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium.

Circulation
Smith, Nicholas L NL; Chen, Ming-Huei MH; Dehghan, Abbas A; Strachan, David P DP; Basu, Saonli S; Soranzo, Nicole N; Hayward, Caroline C; Rudan, Igor I; Sabater-Lleal, Maria M; Bis, Joshua C JC; de Maat, Moniek P M MP; Rumley, Ann A; Kong, Xiaoxiao X; Yang, Qiong Q; Williams, Frances M K FM; Vitart, Veronique V; Campbell, Harry H; Mälarstig, Anders A; Wiggins, Kerri L KL; Van Duijn, Cornelia M CM; McArdle, Wendy L WL; Pankow, James S JS; Johnson, Andrew D AD; Silveira, Angela A; McKnight, Barbara B; Uitterlinden, Andre G AG; , ; Aleksic, Nena N; Meigs, James B JB; Peters, Annette A; Koenig, Wolfgang W; Cushman, Mary M; Kathiresan, Sekar S; Rotter, Jerome I JI; Bovill, Edwin G EG; Hofman, Albert A; Boerwinkle, Eric E; Tofler, Geoffrey H GH; Peden, John F JF; Psaty, Bruce M BM; Leebeek, Frank F; Folsom, Aaron R AR; Larson, Martin G MG; Spector, Timothy D TD; Wright, Alan F AF; Wilson, James F JF; Hamsten, Anders A; Lumley, Thomas T; Witteman, Jacqueline C M JC; Tang, Weihong W; O'Donnell, Christopher J CJ
Publication Date: 2010-03-30

Variant appearance in text: rs488703
PubMed Link: 20231535
Variant Present in the following documents:
  • Main text
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A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose.

Blood
Cooper, Gregory M GM; Johnson, Julie A JA; Langaee, Taimour Y TY; Feng, Hua H; Stanaway, Ian B IB; Schwarz, Ute I UI; Ritchie, Marylyn D MD; Stein, C Michael CM; Roden, Dan M DM; Smith, Joshua D JD; Veenstra, David L DL; Rettie, Allan E AE; Rieder, Mark J MJ
Publication Date: 2008-08-15

Variant appearance in text: rs488703
PubMed Link: 18535201
Variant Present in the following documents:
  • Main text
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Association of warfarin dose with genes involved in its action and metabolism.

Human Genetics
Wadelius, Mia M; Chen, Leslie Y LY; Eriksson, Niclas N; Bumpstead, Suzannah S; Ghori, Jilur J; Wadelius, Claes C; Bentley, David D; McGinnis, Ralph R; Deloukas, Panos P
Publication Date: 2007-03

Variant appearance in text: rs488703
PubMed Link: 17048007
Variant Present in the following documents:
View BVdb publication page