Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs939679843
rs939679843
PRH1 ; PRR4 ; PRH1-PRR4
0.010 GeneticVariation BEFREE We have identified one frameshift (3363 ins C) and two missense mutations (R178Q and T298M) in 7 French Canadian families with type I PROC deficiency. 9798967

1998