Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1481318368
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.090 1.000 9 2013 2020
dbSNP: rs1481318368
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma 		0.010 1.000 1 2003 2003
dbSNP: rs1481318368
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior 		0.010 1.000 1 2018 2018
dbSNP: rs1481318368
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv
CUI: C0851578
Disease: Sleep Disorders
Sleep Disorders 		0.010 1.000 1 2013 2013
dbSNP: rs1481318368
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders 		0.010 1.000 1 2013 2013
dbSNP: rs1481318368
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv
CUI: C0037317
Disease: Sleep disturbances
Sleep disturbances 		0.010 1.000 1 2013 2013
dbSNP: rs1481318368
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma 		0.010 1.000 1 2003 2003
dbSNP: rs1481318368
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv
CUI: C0947785
Disease: [D]Sleep disturbances (& [hypersomnia] or [insomnia])
[D]Sleep disturbances (& [hypersomnia] or [insomnia]) 		0.010 1.000 1 2013 2013
dbSNP: rs1481318368
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma 		0.010 1.000 1 2003 2003
dbSNP: rs1481318368
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv
CUI: C0003467
Disease: Anxiety
Anxiety 		0.010 1.000 1 2013 2013