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: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
Diabetes Mellitus, Non-Insulin-Dependent
0.100 0.841 44 1994 2019
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.100 0.833 18 2001 2017
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.080 1.000 8 2005 2016
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.050 1.000 5 1999 2014
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0011847
Disease: Diabetes
Diabetes
0.050 1.000 5 1999 2014
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0028754
Disease: Obesity
Obesity
0.050 1.000 5 2001 2016
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.030 1.000 3 2009 2011
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.030 1.000 3 2005 2011
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.030 1.000 3 2007 2018
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
Diabetes Mellitus, Insulin-Dependent
0.030 1.000 3 2003 2004
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.030 1.000 3 2014 2019
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.030 1.000 3 2007 2018
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.030 1.000 3 2005 2011
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 1.000 2 2005 2013
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.020 1.000 2 2005 2011
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive
0.020 1.000 2 2006 2016
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 1.000 2 2005 2013
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
Malignant neoplasm of colon and/or rectum
0.020 1.000 2 2014 2016
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
Obstructive sleep apnea hypopnea syndrome
0.010 1.000 1 2016 2016
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.010 1.000 1 2004 2004
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2014 2014
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
Hyperlipidemia, Familial Combined
0.010 1.000 1 2002 2002
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 1.000 1 2016 2016
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0014556
Disease: Epilepsy, Temporal Lobe
Epilepsy, Temporal Lobe
0.010 1.000 1 2015 2015