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: rs138663667
rs138663667 		1.000 0.080 7 82276774 intron variant G/T snv 0.13
CUI: C0220633
Disease: Uveal melanoma
Uveal melanoma 		Neoplasms; Eye Diseases 0.700 1.000 1 2020 2020
dbSNP: rs17155782
rs17155782 		1.000 0.040 7 82041719 intron variant G/A snv 0.14
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17156195
rs17156195 		0.925 0.040 7 82351854 intron variant T/A snv 2.3E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs17156195
rs17156195 		0.925 0.040 7 82351854 intron variant T/A snv 2.3E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs17156280
rs17156280 		0.925 0.040 7 82414674 intron variant T/C snv 3.4E-02
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2016 2016
dbSNP: rs17156280
rs17156280 		0.925 0.040 7 82414674 intron variant T/C snv 3.4E-02
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		Mental Disorders 0.700 1.000 1 2016 2016
dbSNP: rs17176546
rs17176546 		1.000 0.040 7 82251598 intron variant G/A snv 2.8E-02
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs2237505
rs2237505 		1.000 0.040 7 82061610 intron variant C/T snv 0.32
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs2367841
rs2367841 		1.000 0.040 7 82042943 intron variant A/G snv 0.49
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs6942458
rs6942458 		7 82153198 intron variant A/G snv 0.28
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2012 2012
dbSNP: rs6942458
rs6942458 		7 82153198 intron variant A/G snv 0.28
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs6970802
rs6970802 		1.000 0.040 7 82041949 intron variant C/T snv 0.30
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11567245
rs11567245 		1.000 0.120 7 82151406 intron variant T/A snv
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.010 < 0.001 1 2019 2019