F5 c.730+316G>A

Variant ID: 1-169528075-C-T

NM_000130.4(F5):c.730+316G>A

This variant was identified in 3 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: rs9332570
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



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: rs9332570
PubMed Link: 23662219
Variant Present in the following documents:
  • Main text
  • CRIM.GENETICS2013-941684.pdf
View BVdb publication page



Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe).

Investigative Ophthalmology & Visual Science
Sobrin, Lucia L; Green, Todd T; Sim, Xueling X; Jensen, Richard A RA; Tai, E Shyong ES; Tay, Wan Ting WT; Wang, Jie Jin JJ; Mitchell, Paul P; Sandholm, Niina N; Liu, Yiyuan Y; Hietala, Kustaa K; Iyengar, Sudha K SK; , ; Brooks, Matthew M; Buraczynska, Monika M; Van Zuydam, Natalie N; Smith, Albert V AV; Gudnason, Vilmundur V; Doney, Alex S F AS; Morris, Andrew D AD; Leese, Graham P GP; Palmer, Colin N A CN; , ; Swaroop, Anand A; Taylor, Herman A HA; Wilson, James G JG; Penman, Alan A; Chen, Ching J CJ; Groop, Per-Henrik PH; Saw, Seang-Mei SM; Aung, Tin T; Klein, Barbara E BE; Rotter, Jerome I JI; Siscovick, David S DS; Cotch, Mary Frances MF; Klein, Ronald R; Daly, Mark J MJ; Wong, Tien Y TY
Publication Date: 2011-09-29

Variant appearance in text: rs9332570
PubMed Link: 21873659
Variant Present in the following documents:
  • Main text
View BVdb publication page