INS, insulin, 3630

N. diseases: 405; N. variants: 37
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: rs689
rs689
0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.790 1.000 12 2009 2019
dbSNP: rs689
rs689
0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.720 1.000 3 2016 2019
dbSNP: rs689
rs689
0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60
Latent autoimmune diabetes mellitus in adult
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.020 1.000 2 2008 2019
dbSNP: rs689
rs689
0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60
Latent Autoimmune Diabetes in Adults
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.710 1.000 2 2018 2019
dbSNP: rs689
rs689
0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement
0.700 1.000 1 2011 2011
dbSNP: rs689
rs689
0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs689
rs689
0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
Autoimmune thyroid disease (AITD)
0.010 1.000 1 2009 2009
dbSNP: rs689
rs689
0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs689
rs689
0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60
Adenocarcinoma of the gastroesophageal junction
Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs121908260
rs121908260
0.851 0.160 11 2160835 missense variant C/T snv
Maturity-onset diabetes of the young, type 10
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.800 1.000 4 2008 2014
dbSNP: rs121908260
rs121908260
0.851 0.160 11 2160835 missense variant C/T snv
CUI: C3888631
Disease: Monogenic diabetes
Monogenic diabetes
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs121908260
rs121908260
0.851 0.160 11 2160835 missense variant C/T snv
CUI: C0021670
Disease: insulinoma
insulinoma
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs121908260
rs121908260
0.851 0.160 11 2160835 missense variant C/T snv
Maturity onset diabetes mellitus in young
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs121908261
rs121908261
0.851 0.120 11 2160809 missense variant G/A snv
DIABETES MELLITUS, INSULIN-DEPENDENT, 2
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.800 1.000 1 2008 2008
dbSNP: rs121908261
rs121908261
0.851 0.120 11 2160809 missense variant G/A snv
CUI: C0011847
Disease: Diabetes
Diabetes
Endocrine System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs121908261
rs121908261
0.851 0.120 11 2160809 missense variant G/A snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs121908261
rs121908261
0.851 0.120 11 2160809 missense variant G/A snv
CUI: C0022638
Disease: Ketosis
Ketosis
Nutritional and Metabolic Diseases 0.010 1.000 1 2008 2008
dbSNP: rs121908261
rs121908261
0.851 0.120 11 2160809 missense variant G/A snv
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs80356664
rs80356664
0.882 0.120 11 2160878 missense variant C/G;T snv
DIABETES MELLITUS, PERMANENT NEONATAL
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.800 1.000 2 2007 2008
dbSNP: rs80356664
rs80356664
0.882 0.120 11 2160878 missense variant C/G;T snv
CUI: C0011847
Disease: Diabetes
Diabetes
Endocrine System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs80356664
rs80356664
0.882 0.120 11 2160878 missense variant C/G;T snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
Immune System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs80356664
rs80356664
0.882 0.120 11 2160878 missense variant C/G;T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs80356664
rs80356664
0.882 0.120 11 2160878 missense variant C/G;T snv
DIABETES MELLITUS, INSULIN-DEPENDENT, 2
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 0
dbSNP: rs1057524907
rs1057524907
0.925 0.080 11 2159907 missense variant T/C snv
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
Nutritional and Metabolic Diseases 0.700 1.000 5 2007 2015
dbSNP: rs1057524907
rs1057524907
0.925 0.080 11 2159907 missense variant T/C snv
CUI: C3888631
Disease: Monogenic diabetes
Monogenic diabetes
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 5 2007 2015