Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0041105
Disease: Trismus
Trismus
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0598275
Disease: Diffuse cerebral atrophy
Diffuse cerebral atrophy
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C1849097
Disease: Loss of ability to walk
Loss of ability to walk
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C1843175
Disease: Hyperreflexia in upper limbs
Hyperreflexia in upper limbs
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C1861239
Disease: Plantar flexion contractures
Plantar flexion contractures
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0497327
Disease: Dementia
Dementia
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0333068
Disease: Flexion contracture
Flexion contracture
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0409345
Disease: Flexion contracture - wrist
Flexion contracture - wrist
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C1850601
Disease: Abnormality of brainstem morphology
Abnormality of brainstem morphology
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0034372
Disease: Quadriplegia
Quadriplegia
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0240914
Disease: Romberg's sign positive
Romberg's sign positive
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0027066
Disease: Myoclonus
Myoclonus
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C1836003
Disease: Facial diplegia
Facial diplegia
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0426970
Disease: Spastic Quadriplegia
Spastic Quadriplegia
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0015310
Disease: Exotropia
Exotropia
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 0