Variant: rs312262717 

    present in Gene: SPG11
    present in Chromosome: 15
    Position on Chromosome: 44659104
    Alleles of this Variant: A/-;AA

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

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

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.

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

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

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

rs312262717 in SPG11 gene and Loss of ability to walk PMID 19194956 2009 SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration.

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

rs312262717 in SPG11 gene and Melanocortin 4 Receptor Deficiency PMID 19194956 2009 SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration.

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

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

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

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

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

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

rs312262717 in SPG11 gene and Spastic paraplegia 11, autosomal recessive PMID 19194956 2009 SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration.

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

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.