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: rs1553456695
rs1553456695
1.000 0.040 2 156329859 frameshift variant -/C delins
CUI: C0014544
Disease: Epilepsy
Epilepsy
Nervous System Diseases 0.700 0
dbSNP: rs35479735
rs35479735
1.000 0.040 2 156326700 intron variant C/- delins 0.71 0.79
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.020 0.500 2 2017 2017
dbSNP: rs1453063924
rs1453063924
1.000 0.040 2 156329978 missense variant C/T snv 4.0E-06
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2005 2005