SPP1, secreted phosphoprotein 1, 6696

N. diseases: 824; N. variants: 13
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: rs4754
rs4754
0.752 0.360 4 87981540 missense variant T/A;C snv 0.32
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
Nervous System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs4754
rs4754
0.752 0.360 4 87981540 missense variant T/A;C snv 0.32
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs4754
rs4754
0.752 0.360 4 87981540 missense variant T/A;C snv 0.32
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs4754
rs4754
0.752 0.360 4 87981540 missense variant T/A;C snv 0.32
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs4754
rs4754
0.752 0.360 4 87981540 missense variant T/A;C snv 0.32
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs4754
rs4754
0.752 0.360 4 87981540 missense variant T/A;C snv 0.32
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs4754
rs4754
0.752 0.360 4 87981540 missense variant T/A;C snv 0.32
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs4754
rs4754
0.752 0.360 4 87981540 missense variant T/A;C snv 0.32
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs4754
rs4754
0.752 0.360 4 87981540 missense variant T/A;C snv 0.32
CUI: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs4754
rs4754
0.752 0.360 4 87981540 missense variant T/A;C snv 0.32
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: rs4754
rs4754
0.752 0.360 4 87981540 missense variant T/A;C snv 0.32
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs4754
rs4754
0.752 0.360 4 87981540 missense variant T/A;C snv 0.32
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs9138
rs9138
0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.020 1.000 2 2013 2014
dbSNP: rs9138
rs9138
0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.020 1.000 2 2013 2017
dbSNP: rs9138
rs9138
0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.020 0.500 2 2014 2015
dbSNP: rs9138
rs9138
0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs9138
rs9138
0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs9138
rs9138
0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs9138
rs9138
0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs9138
rs9138
0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv
CUI: C0035851
Disease: Root Resorption
Root Resorption
Stomatognathic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs9138
rs9138
0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs9138
rs9138
0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs9138
rs9138
0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs9138
rs9138
0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs11730582
rs11730582
0.807 0.240 4 87975269 non coding transcript exon variant T/C snv 0.37
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip
Musculoskeletal Diseases 0.010 < 0.001 1 2015 2015