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: rs2481665
rs2481665 		1 62129005 intron variant T/C snv 0.31
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2015 2018
dbSNP: rs12140153
rs12140153 		1 62114219 missense variant G/A;T snv 4.0E-06; 5.9E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2019 2019
dbSNP: rs12140153
rs12140153 		1 62114219 missense variant G/A;T snv 4.0E-06; 5.9E-02
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		0.700 1.000 2 2016 2017
dbSNP: rs1056513
rs1056513 		1 61914626 missense variant G/A;C snv 0.57; 8.0E-06
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs1056513
rs1056513 		1 61914626 missense variant G/A;C snv 0.57; 8.0E-06
CUI: C0005910
Disease: Body Weight
Body Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2012 2012
dbSNP: rs1056513
rs1056513 		1 61914626 missense variant G/A;C snv 0.57; 8.0E-06
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2012 2012
dbSNP: rs11207881
rs11207881 		0.925 0.040 1 61973715 intron variant T/C snv 3.9E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs11207881
rs11207881 		0.925 0.040 1 61973715 intron variant T/C snv 3.9E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs12140153
rs12140153 		1 62114219 missense variant G/A;T snv 4.0E-06; 5.9E-02
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs12140153
rs12140153 		1 62114219 missense variant G/A;T snv 4.0E-06; 5.9E-02
CUI: C0518026
Disease: body fat percentage (physical finding)
body fat percentage (physical finding) 		0.700 1.000 1 2019 2019
dbSNP: rs12140153
rs12140153 		1 62114219 missense variant G/A;T snv 4.0E-06; 5.9E-02
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2017 2017
dbSNP: rs2481665
rs2481665 		1 62129005 intron variant T/C snv 0.31
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs2666504
rs2666504 		1 62169409 intron variant T/C snv 0.47
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs41313250
rs41313250 		1 62017951 splice region variant A/G snv 9.5E-02 8.4E-02
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs76221407
rs76221407 		1.000 0.080 1 62131826 intron variant A/G snv 3.1E-02
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2019 2019