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: rs188286943
rs188286943
0.776 0.160 16 46662452 missense variant C/T snv
Autosomal dominant late onset Parkinson disease
Nervous System Diseases 0.020 1.000 2 2011 2017
dbSNP: rs3743928
rs3743928
1.000 0.040 16 46689167 5 prime UTR variant C/A;G;T snv 8.1E-05; 4.5E-06; 3.2E-05; 3.3E-03
Autosomal dominant late onset Parkinson disease
Nervous System Diseases 0.010 < 0.001 1 2012 2012