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: rs2044029
rs2044029 		15 71387620 intron variant A/G snv 0.61
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		0.800 1.000 1 2012 2012
dbSNP: rs12899618
rs12899618 		15 71352781 intron variant G/A snv 0.14
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		0.700 1.000 2 2010 2012
dbSNP: rs1441358
rs1441358 		1.000 0.040 15 71320175 intron variant T/G snv 0.38
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.700 1.000 2 2017 2019
dbSNP: rs11631778
rs11631778 		15 71314041 intron variant G/A snv 0.59
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2017 2017
dbSNP: rs11855326
rs11855326 		15 71318496 intron variant G/A snv 0.31
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding) 		0.700 1.000 1 2014 2014
dbSNP: rs11855326
rs11855326 		15 71318496 intron variant G/A snv 0.31
CUI: C0231921
Disease: Pulmonary function
Pulmonary function 		0.700 1.000 1 2014 2014
dbSNP: rs11858540
rs11858540 		15 71330447 intron variant T/G snv 0.14
CUI: C0231921
Disease: Pulmonary function
Pulmonary function 		0.700 1.000 1 2014 2014
dbSNP: rs11858540
rs11858540 		15 71330447 intron variant T/G snv 0.14
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding) 		0.700 1.000 1 2014 2014
dbSNP: rs12102112
rs12102112 		1.000 0.040 15 71363396 intron variant C/T snv 0.13
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.700 1.000 1 2019 2019
dbSNP: rs12441227
rs12441227 		15 71404547 intron variant A/G snv 0.14
CUI: C0231921
Disease: Pulmonary function
Pulmonary function 		0.700 1.000 1 2014 2014
dbSNP: rs12441227
rs12441227 		15 71404547 intron variant A/G snv 0.14
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		0.700 1.000 1 2014 2014
dbSNP: rs12441227
rs12441227 		15 71404547 intron variant A/G snv 0.14
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding) 		0.700 1.000 1 2014 2014
dbSNP: rs12899618
rs12899618 		15 71352781 intron variant G/A snv 0.14
CUI: C0231921
Disease: Pulmonary function
Pulmonary function 		0.700 1.000 1 2010 2010
dbSNP: rs12899618
rs12899618 		15 71352781 intron variant G/A snv 0.14
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding) 		0.700 1.000 1 2010 2010
dbSNP: rs12899618
rs12899618 		15 71352781 intron variant G/A snv 0.14
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2012 2012
dbSNP: rs142200609
rs142200609 		1.000 0.080 15 71449755 intron variant C/T snv 1.1E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2016 2016
dbSNP: rs1441357
rs1441357 		0.925 0.040 15 71320058 intron variant G/A snv 8.4E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs1441357
rs1441357 		0.925 0.040 15 71320058 intron variant G/A snv 8.4E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1441358
rs1441358 		1.000 0.040 15 71320175 intron variant T/G snv 0.38
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2019 2019
dbSNP: rs1441358
rs1441358 		1.000 0.040 15 71320175 intron variant T/G snv 0.38
CUI: C1518922
Disease: peak expiratory flow (procedure)
peak expiratory flow (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs1441361
rs1441361 		15 71332783 intron variant A/G snv 0.15
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding) 		0.700 1.000 1 2014 2014
dbSNP: rs1441361
rs1441361 		15 71332783 intron variant A/G snv 0.15
CUI: C0231921
Disease: Pulmonary function
Pulmonary function 		0.700 1.000 1 2014 2014
dbSNP: rs17786786
rs17786786 		15 71316280 intron variant A/C snv 0.32
CUI: C0231921
Disease: Pulmonary function
Pulmonary function 		0.700 1.000 1 2014 2014
dbSNP: rs17786786
rs17786786 		15 71316280 intron variant A/C snv 0.32
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding) 		0.700 1.000 1 2014 2014
dbSNP: rs1837762
rs1837762 		15 71319964 intron variant G/A snv 0.14
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding) 		0.700 1.000 1 2014 2014