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: rs11191270
rs11191270 		10 102364848 intron variant C/T snv 0.16
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 3 2018 2019
dbSNP: rs12772375
rs12772375 		10 102322931 intron variant T/G snv 0.48
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2019
dbSNP: rs72845660
rs72845660 		10 102312216 intron variant C/A;G snv
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2019
dbSNP: rs144625846
rs144625846 		10 102318287 intron variant A/G snv 9.2E-02
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2019 2019
dbSNP: rs2296887
rs2296887 		1.000 0.040 10 102245653 5 prime UTR variant T/C snv 0.11
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs2485371
rs2485371 		10 102274330 intron variant T/C snv 0.34
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs2485376
rs2485376 		10 102290249 intron variant G/A snv 0.33
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2014 2014
dbSNP: rs4919624
rs4919624 		10 102261328 intron variant A/G snv 0.16
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs72845655
rs72845655 		10 102284277 intron variant A/G snv 1.6E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs72845663
rs72845663 		10 102321592 intron variant C/T snv 0.32
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs772031
rs772031 		10 102261784 intron variant A/C;G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs3758549
rs3758549 		0.882 0.040 10 102244438 upstream gene variant G/A snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.100 0.818 11 2009 2014
dbSNP: rs3758549
rs3758549 		0.882 0.040 10 102244438 upstream gene variant G/A snv 0.14
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease 		Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs3758549
rs3758549 		0.882 0.040 10 102244438 upstream gene variant G/A snv 0.14
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		Nervous System Diseases 0.010 < 0.001 1 2017 2017