Gene: PRH2 ×
Source: BEFREE ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs764734814
rs764734814
PRH1 ; PRH2 ; PRR4 ; PRH1-PRR4
0.010 GeneticVariation BEFREE This study aimed to explore the mechanism of a novel mutation (p.Lys38Glu) in apolipoprotein H (APOH) gene causing hereditary beta2-glycoprotein I (β2GPI) deficiency and thrombosis in a proband with thrombophilia. 30074200

2018