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.