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: rs113994099
rs113994099
0.827 0.240 15 89320883 missense variant T/C snv
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders
Nervous System Diseases 0.020 1.000 2 2007 2013
dbSNP: rs113994097
rs113994097
0.724 0.400 15 89323426 missense variant C/G snv 9.7E-04 7.9E-04
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders
Nervous System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs41549716
rs41549716
0.882 0.200 15 89321842 missense variant T/C snv 6.6E-03 7.0E-03
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders
Nervous System Diseases 0.010 1.000 1 2007 2007