F2 c.559+793C>G

Variant ID: 11-46745861-C-G

NM_000506.3(F2):c.559+793C>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Association between human prothrombin variant (T165M) and kidney stone disease.

Plos One
Rungroj, Nanyawan N; Sudtachat, Nirinya N; Nettuwakul, Choochai C; Sawasdee, Nunghathai N; Praditsap, Oranud O; Jungtrakoon, Prapaporn P; Sritippayawan, Suchai S; Chuawattana, Duangporn D; Borvornpadungkitti, Sombat S; Predanon, Chagkrapan C; Susaengrat, Wattanachai W; Yenchitsomanus, Pa-Thai PT
Publication Date: 2012

Variant appearance in text: rs3136456
PubMed Link: 23029076
Variant Present in the following documents:
  • Main text
  • pone.0045533.pdf
View BVdb publication page



Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.

Human Molecular Genetics
Drenos, Fotios F; Talmud, Philippa J PJ; Casas, Juan P JP; Smeeth, Liam L; Palmen, Jutta J; Humphries, Steve E SE; Hingorani, Aroon D AD
Publication Date: 2009-06-15

Variant appearance in text: rs3136456
PubMed Link: 19336475
Variant Present in the following documents:
  • ddp159_1.pdf
View BVdb publication page