Disease | N. SNPs d | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AFEXOME | AFGENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Spastic Paraplegia, Hereditary
|
41 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.720 | 1.000 | 15 | 2006 | 2018 | ||||
Movement Disorders
|
247 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.700 | 1.000 | 13 | 2012 | 2017 | ||||
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
38 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.800 | 1.000 | 8 | 2006 | 2016 | ||||
Ataxia
|
68 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.720 | 1.000 | 3 | 2016 | 2019 | ||||
Cerebellar Ataxia
|
120 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.020 | 1.000 | 2 | 2019 | 2019 | ||||
Henoch-Schoenlein Purpura
|
59 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.020 | 1.000 | 2 | 2006 | 2013 | ||||
Dysarthria
|
54 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
Muscle Spasticity
|
48 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
Nystagmus
|
95 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
Paraparesis, Spastic
|
37 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.710 | 1.000 | 1 | 2012 | 2012 | ||||
Spastic Ataxia
|
3 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||
Spastic Paraplegia
|
93 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
Spastic Paraplegia Type 7
|
2 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
Abnormal delivery
|
37 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.700 | 0 | |||||||
Abnormality of the optic nerve
|
11 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.700 | 0 | |||||||
Ankle clonus
|
5 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.700 | 0 | |||||||
ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION
|
3 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.700 | 0 | |||||||
Cerebellar ataxia associated with quadrupedal gait
|
1 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.700 | 0 | |||||||
Cerebral cortical atrophy
|
13 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.700 | 0 | |||||||
Compression of spinal cord
|
2 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.700 | 0 | |||||||
Diffuse cerebellar atrophy
|
4 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.700 | 0 | |||||||
Dysdiadochokinesis
|
7 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.700 | 0 | |||||||
Gait abnormality
|
23 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.700 | 0 | |||||||
Gait Ataxia
|
17 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.700 | 0 | |||||||
Gait, Unsteady
|
14 | 0.716 | 0.520 | 16 | 89546737 | missense variant | C/T | snv | 2.9E-03 | 3.5E-03 | 0.700 | 0 |