Source: BEFREE

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: rs2268388
rs2268388
ACACB
0.851 0.200 12 109205840 intron variant G/A snv 0.14
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.050 1.000 5 2010 2018
dbSNP: rs2268388
rs2268388
ACACB
0.851 0.200 12 109205840 intron variant G/A snv 0.14
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		0.040 1.000 4 2013 2015
dbSNP: rs2268388
rs2268388
ACACB
0.851 0.200 12 109205840 intron variant G/A snv 0.14
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.030 1.000 3 2010 2015
dbSNP: rs2268388
rs2268388
ACACB
0.851 0.200 12 109205840 intron variant G/A snv 0.14
CUI: C0011847
Disease: Diabetes
Diabetes 		0.030 1.000 3 2010 2015
dbSNP: rs2241220
rs2241220
ACACB
1.000 0.040 12 109237224 synonymous variant T/A;C;G snv 4.0E-06; 0.83
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia 		0.020 1.000 2 2008 2009
dbSNP: rs2268388
rs2268388
ACACB
0.851 0.200 12 109205840 intron variant G/A snv 0.14
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy 		0.020 1.000 2 2013 2015
dbSNP: rs2239607
rs2239607
ACACB
0.925 0.120 12 109209475 intron variant A/G snv 0.14
CUI: C0028756
Disease: Obesity, Morbid
Obesity, Morbid 		0.010 1.000 1 2011 2011
dbSNP: rs2239607
rs2239607
ACACB
0.925 0.120 12 109209475 intron variant A/G snv 0.14
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.010 1.000 1 2011 2011
dbSNP: rs2239607
rs2239607
ACACB
0.925 0.120 12 109209475 intron variant A/G snv 0.14
CUI: C0011847
Disease: Diabetes
Diabetes 		0.010 1.000 1 2011 2011
dbSNP: rs2241220
rs2241220
ACACB
1.000 0.040 12 109237224 synonymous variant T/A;C;G snv 4.0E-06; 0.83
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.010 1.000 1 2008 2008
dbSNP: rs2268388
rs2268388
ACACB
0.851 0.200 12 109205840 intron variant G/A snv 0.14
CUI: C0028756
Disease: Obesity, Morbid
Obesity, Morbid 		0.010 1.000 1 2011 2011
dbSNP: rs4766587
rs4766587
ACACB
1.000 0.040 12 109247525 intron variant G/A snv 0.23
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.010 1.000 1 2010 2010
dbSNP: rs6606697
rs6606697
ACACB
1.000 0.040 12 109173915 intron variant A/G snv 0.48
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.010 1.000 1 2010 2010