Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs766264810
rs766264810
1.000 0.160 10 95611372 missense variant C/A;T snv 1.2E-05
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder)
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases 0.800 0
dbSNP: rs863224945
rs863224945
1.000 0.160 10 95637381 missense variant A/G snv
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder)
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases 0.800 0
dbSNP: rs864321669
rs864321669
1.000 0.160 10 95633040 missense variant C/G snv
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder)
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases 0.800 1.000 2 2015 2016
dbSNP: rs864321670
rs864321670
0.763 0.320 10 95633012 missense variant C/T snv
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder)
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases 0.800 1.000 2 2015 2016