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: rs4745062
rs4745062 		9 71169348 intron variant C/T snv 0.40
CUI: C0023980
Disease: Longevity
Longevity 		0.800 1.000 1 2010 2010
dbSNP: rs10746862
rs10746862 		9 71165996 intron variant T/A;C;G snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs10780944
rs10780944 		9 70542500 intron variant G/A snv 0.86
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2013 2013
dbSNP: rs10868998
rs10868998 		9 71254839 intron variant A/C;G snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1329767
rs1329767 		9 71183455 intron variant C/A snv 0.35
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs150282530
rs150282530 		1.000 0.040 9 70938329 intron variant C/T snv 9.3E-04
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs2134858
rs2134858 		9 71222239 intron variant C/T snv 0.50
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2309891
rs2309891 		9 71226002 intron variant C/A;G snv
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs2309891
rs2309891 		9 71226002 intron variant C/A;G snv
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs4745021
rs4745021 		1.000 0.080 9 70652691 intron variant T/A;G snv
CUI: C0040137
Disease: Thyroid Nodule
Thyroid Nodule 		Neoplasms; Endocrine System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs59300564
rs59300564 		9 70572040 intron variant C/T snv 2.3E-02
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs71507014
rs71507014 		0.851 0.040 9 70823689 intron variant -/C;CC delins
CUI: C1536085
Disease: Geographic Atrophy
Geographic Atrophy 		Eye Diseases 0.700 1.000 1 2016 2016
dbSNP: rs71507014
rs71507014 		0.851 0.040 9 70823689 intron variant -/C;CC delins
CUI: C2237660
Disease: exudative macular degeneration
exudative macular degeneration 		Eye Diseases 0.700 1.000 1 2016 2016
dbSNP: rs71507014
rs71507014 		0.851 0.040 9 70823689 intron variant -/C;CC delins
CUI: C0271084
Disease: Exudative age-related macular degeneration
Exudative age-related macular degeneration 		Eye Diseases 0.700 1.000 1 2016 2016
dbSNP: rs71507014
rs71507014 		0.851 0.040 9 70823689 intron variant -/C;CC delins
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1564493599
rs1564493599 		1.000 9 70598463 missense variant C/T snv
CUI: C1843367
Disease: Poor school performance
Poor school performance 		0.700 0
dbSNP: rs1564493599
rs1564493599 		1.000 9 70598463 missense variant C/T snv
CUI: C0036572
Disease: Seizures
Seizures 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.700 0
dbSNP: rs1564493599
rs1564493599 		1.000 9 70598463 missense variant C/T snv
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.700 0
dbSNP: rs767146880
rs767146880 		1.000 9 70810048 mature miRNA variant G/A;C snv 4.0E-06
CUI: C4225233
Disease: RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CONGENITAL CATARACT
RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CONGENITAL CATARACT 		0.700 0
dbSNP: rs10780946
rs10780946 		1.000 0.240 9 70548684 intron variant T/C snv 0.48
CUI: C3853540
Disease: Aspirin exacerbated respiratory disease
Aspirin exacerbated respiratory disease 		Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases; Immune System Diseases; Chemically-Induced Disorders; Otorhinolaryngologic Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1328142
rs1328142 		1.000 0.040 9 70783498 intron variant C/A snv 0.21
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.010 1.000 1 2016 2016
dbSNP: rs7025694
rs7025694 		1.000 0.240 9 70550347 intron variant T/C snv 0.48
CUI: C3853540
Disease: Aspirin exacerbated respiratory disease
Aspirin exacerbated respiratory disease 		Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases; Immune System Diseases; Chemically-Induced Disorders; Otorhinolaryngologic Diseases 0.010 < 0.001 1 2016 2016
dbSNP: rs718447
rs718447 		1.000 0.040 9 70811937 intron variant G/A snv 0.31
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs7861254
rs7861254 		1.000 0.040 9 70809868 intron variant C/T snv 0.31
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2015 2015