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.