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
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: 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: 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: 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
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: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.010 < 0.001 1 2019 2019
dbSNP: rs4919510
rs4919510
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27
CUI: C0751075
Disease: Cancer of Digestive System
Cancer of Digestive System
Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2018 2018