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: rs6864049
rs6864049 		5 124994829 intron variant A/C;G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 7 2015 2019
dbSNP: rs4836133
rs4836133 		0.925 0.160 5 124996410 intron variant C/A;G;T snv
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 2 2010 2013
dbSNP: rs4836133
rs4836133 		0.925 0.160 5 124996410 intron variant C/A;G;T snv
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1.000 2 2010 2013
dbSNP: rs10057590
rs10057590 		5 124999554 intron variant A/C snv 0.62
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs116755193
rs116755193 		1.000 0.040 5 124916190 intron variant C/T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs12520745
rs12520745 		1.000 0.120 5 125252697 intron variant C/T snv 0.18
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2014 2014
dbSNP: rs17152484
rs17152484 		1.000 0.120 5 125252465 intron variant C/A;G snv
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2014 2014
dbSNP: rs184897315
rs184897315 		5 125220077 intron variant T/G snv 2.0E-04
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs4240384
rs4240384 		1.000 0.120 5 124955709 intron variant T/C snv 0.85
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis 		Digestive System Diseases; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2019 2019
dbSNP: rs4357030
rs4357030 		5 124980338 non coding transcript exon variant C/T snv 0.72
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs4836133
rs4836133 		0.925 0.160 5 124996410 intron variant C/A;G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2010 2010
dbSNP: rs6864049
rs6864049 		5 124994829 intron variant A/C;G;T snv
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs6889896
rs6889896 		1.000 0.040 5 125363546 intron variant G/A;C;T snv
CUI: C3158111
Disease: response to SSRI
response to SSRI 		0.700 1.000 1 2015 2015
dbSNP: rs6889896
rs6889896 		1.000 0.040 5 125363546 intron variant G/A;C;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2015 2015
dbSNP: rs71576804
rs71576804 		5 125066856 intron variant G/A snv 8.7E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7713414
rs7713414 		0.925 0.040 5 125214387 intron variant C/A;G;T snv 1.8E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs7713414
rs7713414 		0.925 0.040 5 125214387 intron variant C/A;G;T snv 1.8E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs4836133
rs4836133 		0.925 0.160 5 124996410 intron variant C/A;G;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs4836133
rs4836133 		0.925 0.160 5 124996410 intron variant C/A;G;T snv
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2014 2014