Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1224741906
rs1224741906
FN1
0.010 GeneticVariation BEFREE The mutation p.P694L was associated with the same haplotype in five of six families and also detected in two sporadic cases of PCA. 19690585

2010