Variant: rs121965062

present in Gene: SERPINF2 present in Chromosome: 17 Position on Chromosome: 1754289 Alleles of this Variant: G/A

rs121965062 in SERPINF2 gene and ALPHA-2-PLASMIN INHIBITOR DEFICIENCY PMID 2572590 1989 Hereditary alpha 2-plasmin inhibitor deficiency caused by a transport-deficient mutation (alpha 2-PI-Okinawa). Deletion of Glu137 by a trinucleotide deletion blocks intracellular transport.

PMID 10583218 1999 A novel missense mutation in the human plasmin inhibitor (alpha2-antiplasmin) gene associated with a bleeding tendency.