Condition: Fecal Incontinence


rs778361520 in ADGRB2 gene and Fecal Incontinence PMID 28891236 2017 A disease-associated mutation in the adhesion GPCR BAI2 (ADGRB2) increases receptor signaling activity.

rs312262717 in SPG11 gene and Fecal Incontinence PMID 19194956 2009 SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration.