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: rs9324132
rs9324132 		15 26783430 intron variant C/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs4906902
rs4906902 		0.724 0.200 15 26774621 intron variant A/G snv 0.15
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs8179184
rs8179184 		1.000 0.040 15 26774455 intron variant C/A;G;T snv 0.13
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs970408
rs970408 		1.000 0.040 15 26743838 intron variant C/T snv 0.15
CUI: C1842981
Disease: NEUROTICISM
NEUROTICISM 		Behavior and Behavior Mechanisms 0.010 1.000 1 2013 2013
dbSNP: rs1555401440
rs1555401440 		1.000 15 26561149 missense variant G/A snv
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.700 1.000 11 2008 2017
dbSNP: rs1555401440
rs1555401440 		1.000 15 26561149 missense variant G/A snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		Nervous System Diseases 0.700 1.000 11 2008 2017
dbSNP: rs4906902
rs4906902 		0.724 0.200 15 26774621 intron variant A/G snv 0.15
CUI: C0011570
Disease: Mental Depression
Mental Depression 		Behavior and Behavior Mechanisms 0.010 1.000 1 2011 2011
dbSNP: rs1432007
rs1432007 		15 26565542 intron variant A/G;T snv 0.53
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs3212335
rs3212335 		1.000 0.080 15 26766994 intron variant C/T snv 0.32
CUI: C0023980
Disease: Longevity
Longevity 		0.800 1.000 1 2010 2010
dbSNP: rs572427454
rs572427454 		0.882 0.080 15 26560943 missense variant C/T snv 2.8E-05 1.4E-05
CUI: C0238111
Disease: Lennox-Gastaut syndrome
Lennox-Gastaut syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4906902
rs4906902 		0.724 0.200 15 26774621 intron variant A/G snv 0.15
CUI: C0270853
Disease: Juvenile Myoclonic Epilepsy
Juvenile Myoclonic Epilepsy 		Nervous System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs572427454
rs572427454 		0.882 0.080 15 26560943 missense variant C/T snv 2.8E-05 1.4E-05
CUI: C4317339
Disease: Juvenile Absence Epilepsy
Juvenile Absence Epilepsy 		Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs3212335
rs3212335 		1.000 0.080 15 26766994 intron variant C/T snv 0.32
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs4906902
rs4906902 		0.724 0.200 15 26774621 intron variant A/G snv 0.15
CUI: C0270850
Disease: Idiopathic generalized epilepsy
Idiopathic generalized epilepsy 		Nervous System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs3212335
rs3212335 		1.000 0.080 15 26766994 intron variant C/T snv 0.32
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs878960
rs878960 		0.925 0.040 15 26683789 intron variant C/G;T snv
CUI: C3840214
Disease: High-functioning autism
High-functioning autism 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs4906902
rs4906902 		0.724 0.200 15 26774621 intron variant A/G snv 0.15
CUI: C0019337
Disease: Heroin Dependence
Heroin Dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs886037938
rs886037938 		1.000 15 26621417 missense variant C/T snv
CUI: C4310712
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43 		0.800 1.000 6 2013 2017
dbSNP: rs886037939
rs886037939 		1.000 15 26580456 missense variant T/A snv
CUI: C4310712
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43 		0.800 1.000 6 2013 2017
dbSNP: rs886037940
rs886037940 		1.000 15 26567671 missense variant G/T snv
CUI: C4310712
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43 		0.800 1.000 6 2013 2017
dbSNP: rs886037941
rs886037941 		1.000 15 26561099 missense variant C/T snv
CUI: C4310712
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43 		0.800 1.000 6 2013 2017
dbSNP: rs1057519549
rs1057519549 		0.925 0.040 15 26567655 missense variant G/A snv
CUI: C4310712
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43 		0.700 0
dbSNP: rs1057519550
rs1057519550 		0.925 0.040 15 26621403 missense variant T/G snv
CUI: C4310712
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43 		0.700 0
dbSNP: rs1064794797
rs1064794797 		1.000 15 26772403 missense variant A/C;G snv
CUI: C4310712
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43 		0.700 0
dbSNP: rs1064796514
rs1064796514 		1.000 15 26567658 missense variant G/A;T snv
CUI: C4310712
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43 		0.700 0