Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs370103949
rs370103949
FN1
CUI: C0268398
Disease: Familial lichen amyloidosis
Familial lichen amyloidosis 		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