Source: GWASDB

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
0.827 0.240 12 112049014 intron variant A/G snv 0.30
Diabetes Mellitus, Insulin-Dependent
0.810 1.000 3 2007 2010
dbSNP: rs17696736
rs17696736
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 1 2012 2018
dbSNP: rs17696736
rs17696736
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
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 1 2014 2018
dbSNP: rs17696736
rs17696736
0.827 0.240 12 112049014 intron variant A/G snv 0.30
Low density lipoprotein cholesterol measurement
0.800 1.000 1 2012 2018
dbSNP: rs17696736
rs17696736
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
0.827 0.240 12 112049014 intron variant A/G snv 0.30
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs17696736
rs17696736
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
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
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
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