Source: ALL
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: rs121908212
rs121908212
0.732 0.160 19 13303877 missense variant G/A snv
CUI: C0004134
Disease: Ataxia
Ataxia
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.020 1.000 2 2004 2018
dbSNP: rs1057519429
rs1057519429
0.807 0.240 19 13235666 missense variant C/G;T snv
CUI: C0004134
Disease: Ataxia
Ataxia
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1057520918
rs1057520918
0.790 0.160 19 13262780 missense variant C/T snv
CUI: C0004134
Disease: Ataxia
Ataxia
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs121908217
rs121908217
0.851 0.120 19 13308452 missense variant C/T snv 4.0E-06
CUI: C0004134
Disease: Ataxia
Ataxia
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs121908225
rs121908225
0.790 0.120 19 13365448 missense variant G/A snv
CUI: C0004134
Disease: Ataxia
Ataxia
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs121908230
rs121908230
0.882 0.080 19 13262789 missense variant C/T snv
CUI: C0004134
Disease: Ataxia
Ataxia
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2008 2008