MIRLET7E, microRNA let-7e, 406887

N. diseases: 72; N. variants: 3
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: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.020 1.000 2 2018 2019
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.020 1.000 2 2018 2019
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease
Endocrine System Diseases 0.020 1.000 2 2014 2017
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.020 1.000 2 2018 2019
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
CUI: C3714636
Disease: Pneumonitis
Pneumonitis
Infections; Respiratory Tract Diseases 0.020 1.000 2 2018 2019
dbSNP: rs8111742
rs8111742
0.851 0.120 19 51692221 intron variant G/A;C snv 0.30
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
Digestive System Diseases; Neoplasms 0.020 1.000 2 2016 2017
dbSNP: rs8111742
rs8111742
0.851 0.120 19 51692221 intron variant G/A;C snv 0.30
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.020 1.000 2 2016 2017
dbSNP: rs10404453
rs10404453
1.000 0.040 19 51693235 non coding transcript exon variant G/A;C snv 2.6E-03; 5.5E-06
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
Stomatognathic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
CUI: C0018213
Disease: Graves Disease
Graves Disease
Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
CUI: C0342257
Disease: Complications of Diabetes Mellitus
Complications of Diabetes Mellitus
Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2020 2020
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
CUI: C0158252
Disease: Intervertebral disc disorder
Intervertebral disc disorder
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases 0.010 1.000 1 2016 2016
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
Squamous cell carcinoma of esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2016 2016
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
Stomatognathic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2020 2020
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
CUI: C0497327
Disease: Dementia
Dementia
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs12976445
rs12976445
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs8111742
rs8111742
0.851 0.120 19 51692221 intron variant G/A;C snv 0.30
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2019 2019
dbSNP: rs8111742
rs8111742
0.851 0.120 19 51692221 intron variant G/A;C snv 0.30
CUI: C0017154
Disease: Gastritis, Atrophic
Gastritis, Atrophic
Digestive System Diseases 0.010 1.000 1 2016 2016