Source: ALL

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: rs1800437
rs1800437
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
CUI: C0028754
Disease: Obesity
Obesity
0.810 1.000 2 2013 2019
dbSNP: rs1800437
rs1800437
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
Diabetes Mellitus, Non-Insulin-Dependent
0.710 1.000 2 2017 2018
dbSNP: rs1800437
rs1800437
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 3 2017 2019
dbSNP: rs1800437
rs1800437
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs1800437
rs1800437
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
CUI: C0202098
Disease: Insulin measurement
Insulin measurement
0.700 1.000 1 2017 2017
dbSNP: rs1800437
rs1800437
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2017 2017
dbSNP: rs1800437
rs1800437
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
CUI: C0017741
Disease: Glucose tolerance test
Glucose tolerance test
0.700 1.000 1 2017 2017
dbSNP: rs1800437
rs1800437
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
CUI: C0455829
Disease: Waist Circumference
Waist Circumference
0.700 1.000 1 2019 2019
dbSNP: rs1800437
rs1800437
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
body fat percentage (physical finding)
0.700 1.000 1 2019 2019
dbSNP: rs1800437
rs1800437
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
0.010 1.000 1 2019 2019
dbSNP: rs1800437
rs1800437
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity
0.010 1.000 1 2010 2010
dbSNP: rs1800437
rs1800437
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
CUI: C0018801
Disease: Heart failure
Heart failure
0.010 1.000 1 2019 2019
dbSNP: rs1800437
rs1800437
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.010 1.000 1 2007 2007