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: rs121917815
rs121917815
0.925 0.120 3 186854303 missense variant C/T snv 4.0E-06; 1.2E-05
CUI: C2675519
Disease: Hypoadiponectinemia
Hypoadiponectinemia
0.710 1.000 1 2003 2003
dbSNP: rs2241766
rs2241766
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
Diabetes Mellitus, Non-Insulin-Dependent
0.100 0.900 20 2002 2018
dbSNP: rs266729
rs266729
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
Diabetes Mellitus, Non-Insulin-Dependent
0.100 1.000 14 2009 2019
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
Diabetes Mellitus, Non-Insulin-Dependent
0.100 0.923 13 2009 2019
dbSNP: rs2241766
rs2241766
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.100 0.923 13 2006 2019
dbSNP: rs2241766
rs2241766
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C0028754
Disease: Obesity
Obesity
0.100 0.833 12 2004 2019
dbSNP: rs2241766
rs2241766
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.100 0.727 11 2004 2019
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.090 1.000 9 2012 2019
dbSNP: rs2241766
rs2241766
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.090 0.889 9 2013 2017
dbSNP: rs2241766
rs2241766
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.080 0.875 8 2005 2019
dbSNP: rs2241766
rs2241766
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.080 0.750 8 2006 2019
dbSNP: rs2241766
rs2241766
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.080 0.875 8 2011 2019
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.070 1.000 7 2012 2018
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0028754
Disease: Obesity
Obesity
0.060 1.000 6 2009 2019
dbSNP: rs17300539
rs17300539
0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02
Diabetes Mellitus, Non-Insulin-Dependent
0.060 0.833 6 2011 2019
dbSNP: rs2241766
rs2241766
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.060 1.000 6 2010 2018
dbSNP: rs266729
rs266729
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.060 1.000 6 2010 2017
dbSNP: rs266729
rs266729
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.060 0.833 6 2008 2017
dbSNP: rs266729
rs266729
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.060 0.833 6 2011 2019
dbSNP: rs266729
rs266729
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.060 1.000 6 2010 2019
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.050 0.800 5 2011 2019
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.050 0.800 5 2013 2015
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.050 0.800 5 2013 2015
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.050 0.600 5 2011 2018
dbSNP: rs16861194
rs16861194
0.925 0.120 3 186841636 upstream gene variant A/G snv 0.15
Diabetes Mellitus, Non-Insulin-Dependent
0.050 0.800 5 2009 2018