CD274, CD274 molecule, 29126

N. diseases: 1011; N. variants: 8
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: rs1411262
rs1411262 		9 5459419 intron variant C/T snv 0.33
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4143815
rs4143815 		0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.020 1.000 2 2019 2019
dbSNP: rs4143815
rs4143815 		0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.020 1.000 2 2014 2018
dbSNP: rs4143815
rs4143815 		0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		Neoplasms; Respiratory Tract Diseases 0.020 1.000 2 2017 2017
dbSNP: rs4143815
rs4143815 		0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.020 1.000 2 2019 2019
dbSNP: rs17718883
rs17718883 		1.000 0.080 9 5462876 missense variant C/G snv 3.9E-03 3.5E-03
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs1970000
rs1970000 		1.000 0.200 9 5465036 intron variant C/A;G snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs2297136
rs2297136 		0.925 0.120 9 5467955 3 prime UTR variant G/A snv 0.56
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs2297136
rs2297136 		0.925 0.120 9 5467955 3 prime UTR variant G/A snv 0.56
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2890658
rs2890658 		0.925 0.080 9 5465130 intron variant C/A;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs2890658
rs2890658 		0.925 0.080 9 5465130 intron variant C/A;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs2890658
rs2890658 		0.925 0.080 9 5465130 intron variant C/A;T snv
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs2890658
rs2890658 		0.925 0.080 9 5465130 intron variant C/A;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs4143815
rs4143815 		0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs4143815
rs4143815 		0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs4143815
rs4143815 		0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4143815
rs4143815 		0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4143815
rs4143815 		0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C0013882
Disease: Elephantiasis
Elephantiasis 		Hemic and Lymphatic Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4143815
rs4143815 		0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4143815
rs4143815 		0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs4143815
rs4143815 		0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4143815
rs4143815 		0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs4143815
rs4143815 		0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C1720771
Disease: Testicular Hydrocele
Testicular Hydrocele 		Male Urogenital Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4143815
rs4143815 		0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs4143815
rs4143815 		0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018