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: rs878855336
rs878855336
1.000 0.120 7 93133332 missense variant G/A;T snv 4.0E-06
CUI: C1327919
Disease: Myelocerebellar Disorder
Myelocerebellar Disorder
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Hemic and Lymphatic Diseases 0.800 1.000 1 2016 2016
dbSNP: rs878855337
rs878855337
0.925 0.120 7 93132385 missense variant C/G snv
CUI: C1327919
Disease: Myelocerebellar Disorder
Myelocerebellar Disorder
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Hemic and Lymphatic Diseases 0.800 1.000 1 2016 2016
dbSNP: rs1554341158
rs1554341158
1.000 0.120 7 93133016 missense variant G/A snv
CUI: C1327919
Disease: Myelocerebellar Disorder
Myelocerebellar Disorder
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2017 2017
dbSNP: rs1554341277
rs1554341277
1.000 0.120 7 93133300 missense variant A/G snv
CUI: C1327919
Disease: Myelocerebellar Disorder
Myelocerebellar Disorder
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2017 2017