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: rs4234503
rs4234503 		3 10590994 intron variant C/T snv 0.11
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		0.700 1.000 1 2012 2012
dbSNP: rs6807064
rs6807064 		3 10494087 intron variant C/T snv 0.35
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2008 2008
dbSNP: rs6807064
rs6807064 		3 10494087 intron variant C/T snv 0.35
CUI: C0202174
Disease: blood phenylalanine measurement by Guthrie microbiologic assay
blood phenylalanine measurement by Guthrie microbiologic assay 		0.700 1.000 1 2008 2008
dbSNP: rs703912
rs703912 		3 10349742 intron variant A/G snv 0.20
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs735931
rs735931 		1.000 0.040 3 10483412 intron variant A/G snv 0.60
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs75316710
rs75316710 		1.000 0.040 3 10508052 intron variant A/G snv 2.9E-02
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		Mental Disorders 0.700 1.000 1 2015 2015
dbSNP: rs7633661
rs7633661 		0.925 0.040 3 10508163 intron variant C/T snv 9.6E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs7633661
rs7633661 		0.925 0.040 3 10508163 intron variant C/T snv 9.6E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs9879311
rs9879311 		1.000 0.040 3 10373659 intron variant C/A;T snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs9879311
rs9879311 		1.000 0.040 3 10373659 intron variant C/A;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs9880149
rs9880149 		1.000 0.080 3 10644752 intron variant G/A snv 0.33
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs2278556
rs2278556 		0.925 0.040 3 10360419 intron variant G/A snv 0.34
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs2278556
rs2278556 		0.925 0.040 3 10360419 intron variant G/A snv 0.34
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs241509
rs241509 		1.000 0.040 3 10345375 intron variant C/A;T snv 0.45
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs35678
rs35678 		0.925 0.040 3 10338239 missense variant C/T snv 0.49 0.47
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs35678
rs35678 		0.925 0.040 3 10338239 missense variant C/T snv 0.49 0.47
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs3774180
rs3774180 		1.000 0.040 3 10355304 intron variant T/C snv 0.37
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs61736451
rs61736451 		1.000 0.120 3 10359892 missense variant C/A;T snv 4.0E-06; 1.1E-02
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2005 2005