Variant: rs778361520 

    present in Gene: ADGRB2
    present in Chromosome: 1
    Position on Chromosome: 31728621
    Alleles of this Variant: G/A

rs778361520 in ADGRB2 gene and Abnormality of somatosensory evoked potentials PMID 28891236 2017 A disease-associated mutation in the adhesion GPCR BAI2 (ADGRB2) increases receptor signaling activity.

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

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

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

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

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

rs778361520 in ADGRB2 gene and Progressive spastic paraparesis PMID 28891236 2017 A de novo C-terminal mutation (R1465W) in the adhesion GPCR BAI2 (also known as ADGRB2) was identified in a patient suffering from progressive spastic paraparesis and other neurological symptoms.

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