Condition: Urinary Incontinence


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

rs1555743003 in ASXL3 gene and Urinary Incontinence PMID 27075689 2016 Novel splicing mutation in the ASXL3 gene causing Bainbridge-Ropers syndrome.

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