Variant: rs121913064 

    present in Gene: F13A1
    present in Chromosome: 6
    Position on Chromosome: 6151813
    Alleles of this Variant: C/A;T

rs121913064 in F13A1 gene and Factor Xiii, A Subunit, Deficiency Of PMID 24329762 2014 Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations.

PMID 20179087 2010 Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function.

PMID 24286209 2014 Severe congenital factor XIII deficiency caused by novel W187X and G273V mutations in the F13A gene; diagnosis and classification according to the ISTH/SSC guidelines.

PMID 1353995 1992 Identification of a point mutation in factor XIII A subunit deficiency.

PMID 24889649 2014 Eight novel F13A1 gene missense mutations in patients with mild FXIII deficiency: in silico analysis suggests changes in FXIII-A subunit structure/function.

PMID 27363989 2016 Coagulation Factor XIIIA Subunit Missense Mutations Affect Structure and Function at the Various Steps of Factor XIII Action.