F5 c.158+1409G>C

Variant ID: 1-169554058-C-G

NM_000130.4(F5):c.158+1409G>C

This variant was identified in 9 publications

View GRCh38 version.




Publications:


Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs3753305
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
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Environmental and Genetic Risk Factors Associated with Venous Thromboembolism.

Seminars In Thrombosis And Hemostasis
Crous-Bou, Marta M; Harrington, Laura B LB; Kabrhel, Christopher C
Publication Date: 2016-11

Variant appearance in text: rs3753305
PubMed Link: 27764878
Variant Present in the following documents:
  • Main text
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Targeted next-generation resequencing of f5 gene identifies novel multiple variants pattern in severe hereditary factor v deficiency.

Case Reports In Genetics
Janicki, Piotr K PK; Vaida, Sonia S; Al-Mondhiry, Hamid A B HA
Publication Date: 2013

Variant appearance in text: rs3753305
PubMed Link: 23662219
Variant Present in the following documents:
  • Main text
  • CRIM.GENETICS2013-941684.pdf
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A genome-wide association study of variations in maternal cardiometabolic genes and risk of placental abruption.

International Journal Of Molecular Epidemiology And Genetics
Moore, Amy A; Enquobahrie, Daniel A DA; Sanchez, Sixto E SE; Ananth, Cande V CV; Pacora, Percy N PN; Williams, Michelle A MA
Publication Date: 2012

Variant appearance in text: rs3753305
PubMed Link: 23205182
Variant Present in the following documents:
  • Main text
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Replication of findings on the association of genetic variation in 24 hemostasis genes and risk of incident venous thrombosis.

Journal Of Thrombosis And Haemostasis : Jth
Smith, N L NL; Wiggins, K L KL; Reiner, A P AP; Lange, L A LA; Cushman, M M; Heckbert, S R SR; Lumley, T T; Rice, K M KM; Folsom, A R AR; Psaty, B M BM
Publication Date: 2009-10

Variant appearance in text: rs3753305
PubMed Link: 19682239
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common hemostasis and inflammation gene variants and venous thrombosis in older adults from the Cardiovascular Health Study.

Journal Of Thrombosis And Haemostasis : Jth
Reiner, A P AP; Lange, L A LA; Smith, N L NL; Zakai, N A NA; Cushman, M M; Folsom, A R AR
Publication Date: 2009-09

Variant appearance in text: rs3753305
PubMed Link: 19552680
Variant Present in the following documents:
  • Main text
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Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE.

Genes And Immunity
Morris, D L DL; Graham, R R RR; Erwig, L-P LP; Gaffney, P M PM; Moser, K L KL; Behrens, T W TW; Vyse, T J TJ; Graham, D S Cunninghame DS
Publication Date: 2009-07

Variant appearance in text: rs3753305
PubMed Link: 19404301
Variant Present in the following documents:
  • Main text
View BVdb publication page



Multiple genes for essential-hypertension susceptibility on chromosome 1q.

American Journal Of Human Genetics
Chang, Yen-Pei Christy YP; Liu, Xin X; Kim, James Dae Ok JD; Ikeda, Morna A MA; Layton, Marnie R MR; Weder, Alan B AB; Cooper, Richard S RS; Kardia, Sharon L R SL; Rao, D C DC; Hunt, Steve C SC; Luke, Amy A; Boerwinkle, Eric E; Chakravarti, Aravinda A
Publication Date: 2007-02

Variant appearance in text: rs3753305
PubMed Link: 17236131
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: rs3753305
PubMed Link: 17048007
Variant Present in the following documents:
View BVdb publication page