Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17696736
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.810 1.000 3 2007 2010
dbSNP: rs17696736
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 2 2012 2018
dbSNP: rs17696736
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.800 1.000 2 2014 2018
dbSNP: rs17696736
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 2 2012 2018
dbSNP: rs17696736
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.800 1.000 1 2014 2014
dbSNP: rs17696736
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 2 2016 2018
dbSNP: rs17696736
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs17696736
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs17696736
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs17696736
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs17696736
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs17696736
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs17696736
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2012 2012
dbSNP: rs17696736
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17696736
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.700 1.000 1 2013 2013
dbSNP: rs17696736
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2011 2011
dbSNP: rs17696736
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009
dbSNP: rs17696736
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2018 2018