rs174537, TMEM258;MYRF

N. diseases: 23
Disease: Familial lichen amyloidosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Familial lichen amyloidosis
CUI: C0268398
Disease: Familial lichen amyloidosis
0.010 GeneticVariation BEFREE This study tested the relationship of the genotype of a single nucleotide polymorphism, rs174537, and the methylation status of a CpG site, cg27386326, with PUFA composition, and markers of PUFA biosynthesis in PCA tissue. 27197070 2016