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: rs8067235
rs8067235 		17 81050837 intron variant G/A snv 0.30
CUI: C1285654
Disease: Memory performance
Memory performance 		0.800 1.000 1 2014 2014
dbSNP: rs3935190
rs3935190 		17 81110567 3 prime UTR variant G/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2019 2019
dbSNP: rs140721383
rs140721383 		0.925 0.120 17 81071259 intron variant T/C snv 5.2E-04
CUI: C0018099
Disease: Gout
Gout 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2015 2015
dbSNP: rs140721383
rs140721383 		0.925 0.120 17 81071259 intron variant T/C snv 5.2E-04
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2015 2015
dbSNP: rs140721383
rs140721383 		0.925 0.120 17 81071259 intron variant T/C snv 5.2E-04
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2015 2015
dbSNP: rs4076427
rs4076427 		17 81113737 3 prime UTR variant G/C snv 0.34
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs4969374
rs4969374 		17 81077666 intron variant G/A snv 0.23
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs55748329
rs55748329 		1.000 0.040 17 81071973 intron variant A/G snv 0.15
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs56084168
rs56084168 		1.000 0.040 17 81110774 3 prime UTR variant C/T snv 0.15
CUI: C0003467
Disease: Anxiety
Anxiety 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs62073016
rs62073016 		17 81116398 3 prime UTR variant C/T snv 0.33
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs7502214
rs7502214 		17 81099382 intron variant G/C snv 0.22
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs7502590
rs7502590 		1.000 0.040 17 81108281 non coding transcript exon variant A/G snv 0.14
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs7502590
rs7502590 		1.000 0.040 17 81108281 non coding transcript exon variant A/G snv 0.14
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs3934492
rs3934492 		1.000 0.040 17 81060164 intron variant C/G snv 0.32
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs4969239
rs4969239 		0.882 0.120 17 81036744 intron variant A/G snv 0.11
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs4969239
rs4969239 		0.882 0.120 17 81036744 intron variant A/G snv 0.11
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs4969239
rs4969239 		0.882 0.120 17 81036744 intron variant A/G snv 0.11
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs4969385
rs4969385 		1.000 0.040 17 81095090 intron variant C/T snv 0.22
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs8079626
rs8079626 		1.000 0.040 17 81053072 intron variant A/G snv 0.31
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs9913477
rs9913477 		0.925 0.080 17 81041898 intron variant A/C;G snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs9913477
rs9913477 		0.925 0.080 17 81041898 intron variant A/C;G snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018