rs1801278, IRS1

N. diseases: 38
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO
CUI: C1840169
Disease: CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO
3 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.700 0
INSULIN RESISTANCE, SUSCEPTIBILITY TO
CUI: C1852091
Disease: INSULIN RESISTANCE, SUSCEPTIBILITY TO
3 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.700 0
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.100 0.841 44 1994 2019
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.100 0.833 18 2001 2017
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.080 1.000 8 2005 2016
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.050 1.000 5 1999 2014
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.050 1.000 5 1999 2014
Obesity
CUI: C0028754
Disease: Obesity
1111 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.050 1.000 5 2001 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.030 1.000 3 2007 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.030 1.000 3 2014 2019
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.030 1.000 3 2003 2004
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.030 1.000 3 2007 2018
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.030 1.000 3 2005 2011
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.030 1.000 3 2009 2011
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.030 1.000 3 2005 2011
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.020 1.000 2 2005 2011
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.020 1.000 2 2014 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.020 1.000 2 2005 2013
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.020 1.000 2 2005 2013
Sleep Apnea, Obstructive
CUI: C0520679
Disease: Sleep Apnea, Obstructive
105 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.020 1.000 2 2006 2016
21-hydroxylase deficiency
CUI: C0852654
Disease: 21-hydroxylase deficiency
28 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.010 1.000 1 2009 2009
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.010 1.000 1 2014 2014
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.010 1.000 1 2013 2013
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.010 1.000 1 2004 2004
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
CUI: C2936858
Disease: Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
62 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.010 1.000 1 2009 2009