SEMA4G, semaphorin 4G, 57715

N. diseases: 8; 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: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.050 0.600 5 2012 2018
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.050 0.800 5 2015 2019
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.050 0.800 5 2015 2019
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.050 0.800 5 2015 2019
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.050 0.800 5 2012 2018
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.050 0.600 5 2012 2018
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.040 0.750 4 2017 2018
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.040 0.750 4 2017 2018
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.030 1.000 3 2015 2018
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
Malignant neoplasm of colon and/or rectum
0.030 0.667 3 2012 2018
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.020 1.000 2 2013 2015
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.020 0.500 2 2014 2016
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.020 1.000 2 2015 2016
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C3887461
Disease: Head and Neck Carcinoma
Head and Neck Carcinoma
Neoplasms 0.020 1.000 2 2017 2018
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
Malignant Head and Neck Neoplasm
Neoplasms 0.020 1.000 2 2017 2018
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C0243026
Disease: Sepsis
Sepsis
Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2015 2015
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
Squamous cell carcinoma of the head and neck
Neoplasms 0.010 < 0.001 1 2016 2016
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C1960398
Disease: HER2-positive carcinoma of breast
HER2-positive carcinoma of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2012 2012
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
Mucocutaneous Lymph Node Syndrome
Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C0036690
Disease: Septicemia
Septicemia
Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2015 2015
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
Squamous cell carcinoma of esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C1623038
Disease: Cirrhosis
Cirrhosis
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2016 2016
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
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: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C0154038
Disease: Benign neoplasm of thyroid gland
Benign neoplasm of thyroid gland
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2015 2015