IRS1, insulin receptor substrate 1, 3667

N. diseases: 233; N. variants: 15
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1259467443
rs1259467443
1.000 0.080 2 226796570 inframe deletion ACC/- delins 8.0E-06 7.0E-06
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 0
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
INSULIN RESISTANCE, SUSCEPTIBILITY TO
0.700 0
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO
0.700 0
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
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.100 0.841 44 1994 2019
dbSNP: rs1801276
rs1801276
0.882 0.160 2 226797205 missense variant C/G snv 1.4E-02 1.3E-02
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.060 0.833 6 1994 2011
dbSNP: rs1801118
rs1801118
1.000 0.080 2 226798113 missense variant A/G snv 5.6E-05 2.1E-05
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 1996 1996
dbSNP: rs1801120
rs1801120
1.000 0.080 2 226796313 missense variant G/A snv 4.0E-06
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 1996 1996
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance
Nutritional and Metabolic Diseases 0.010 1.000 1 1998 1998
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
Nutritional and Metabolic Diseases; Endocrine System Diseases 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
Endocrine System Diseases 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: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 1999 1999
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
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 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: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 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: C0206081
Disease: Hyperandrogenism
Hyperandrogenism
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 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: C0020474
Disease: Hyperlipidemia, Familial Combined
Hyperlipidemia, Familial Combined
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 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: C0342541
Disease: Precocious pubarche
Precocious pubarche
Endocrine System Diseases 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
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.030 1.000 3 2003 2004
dbSNP: rs104893642
rs104893642
1.000 0.080 2 226796916 missense variant G/A;C snv 1.5E-05; 5.0E-06
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.710 1.000 1 2003 2003
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
Digestive System Diseases; Neoplasms 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: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
Digestive System Diseases; Neoplasms 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: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 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: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 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: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 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: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 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: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.020 1.000 2 2005 2013