MIR218-2, microRNA 218-2, 407001

N. diseases: 19; N. variants: 1
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: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.040 1.000 4 2010 2017
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.040 0.750 4 2014 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.040 0.750 4 2014 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.030 0.667 3 2012 2014
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.030 1.000 3 2010 2017
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C4048328
Disease: cervical cancer
cervical cancer 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.030 1.000 3 2010 2017
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2014 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C1512409
Disease: Hepatocarcinogenesis
Hepatocarcinogenesis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2014 2014
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
Cervical Intraepithelial Neoplasia 		Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
Mucocutaneous Lymph Node Syndrome 		Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.010 < 0.001 1 2018 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma 		Neoplasms; Nervous System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 < 0.001 1 2013 2013
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2013 2013