FMN1, formin 1, 342184

N. diseases: 29; N. variants: 6
Disease: POLYPOSIS SYNDROME, HEREDITARY MIXED, 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1832587
Disease: POLYPOSIS SYNDROME, HEREDITARY MIXED, 1
POLYPOSIS SYNDROME, HEREDITARY MIXED, 1 		0.010 GeneticVariation disease BEFREE We mapped a high-penetrance gene (CRAC1; also known as HMPS) associated with colorectal cancer (CRC) in the Ashkenazi population to a 0.6-Mb region on chromosome 15 containing SCG5 (also known as SGNE1), GREM1 and FMN1. 18084292 2008