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: rs1126616
rs1126616
0.827 0.280 4 87982701 synonymous variant C/G;T snv 0.32 0.26
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs1126616
rs1126616
0.827 0.280 4 87982701 synonymous variant C/G;T snv 0.32 0.26
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: rs1126616
rs1126616
0.827 0.280 4 87982701 synonymous variant C/G;T snv 0.32 0.26
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
Nervous System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1126616
rs1126616
0.827 0.280 4 87982701 synonymous variant C/G;T snv 0.32 0.26
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1126616
rs1126616
0.827 0.280 4 87982701 synonymous variant C/G;T snv 0.32 0.26
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs1126772
rs1126772
0.851 0.320 4 87983034 3 prime UTR variant A/G snv 0.16
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs1126772
rs1126772
0.851 0.320 4 87983034 3 prime UTR variant A/G snv 0.16
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs1126772
rs1126772
0.851 0.320 4 87983034 3 prime UTR variant A/G snv 0.16
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: rs1126772
rs1126772
0.851 0.320 4 87983034 3 prime UTR variant A/G snv 0.16
CUI: C0003165
Disease: Anthracosis
Anthracosis
Respiratory Tract Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1126772
rs1126772
0.851 0.320 4 87983034 3 prime UTR variant A/G snv 0.16
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs11728697
rs11728697
0.925 0.080 4 87977789 non coding transcript exon variant C/T snv 0.54 0.46
CUI: C0003165
Disease: Anthracosis
Anthracosis
Respiratory Tract Diseases 0.010 1.000 1 2015 2015
dbSNP: rs11728697
rs11728697
0.925 0.080 4 87977789 non coding transcript exon variant C/T snv 0.54 0.46
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
Nervous System Diseases 0.010 1.000 1 2016 2016
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
dbSNP: rs11730582
rs11730582
0.807 0.240 4 87975269 non coding transcript exon variant T/C snv 0.37
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs11730582
rs11730582
0.807 0.240 4 87975269 non coding transcript exon variant T/C snv 0.37
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue 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
Secondary malignant neoplasm of lymph node
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs11730582
rs11730582
0.807 0.240 4 87975269 non coding transcript exon variant T/C snv 0.37
CUI: C0334037
Disease: Intestinal metaplasia
Intestinal metaplasia
0.010 1.000 1 2017 2017
dbSNP: rs11730582
rs11730582
0.807 0.240 4 87975269 non coding transcript exon variant T/C snv 0.37
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue 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: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs11730582
rs11730582
0.807 0.240 4 87975269 non coding transcript exon variant T/C snv 0.37
CUI: C0035851
Disease: Root Resorption
Root Resorption
Stomatognathic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs11730582
rs11730582
0.807 0.240 4 87975269 non coding transcript exon variant T/C snv 0.37
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs11730582
rs11730582
0.807 0.240 4 87975269 non coding transcript exon variant T/C snv 0.37
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs17524488
rs17524488
0.925 0.040 4 87975555 non coding transcript exon variant -/G delins
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs17524488
rs17524488
0.925 0.040 4 87975555 non coding transcript exon variant -/G delins
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip
Musculoskeletal Diseases 0.010 1.000 1 2015 2015
dbSNP: rs17524488
rs17524488
0.925 0.040 4 87975555 non coding transcript exon variant -/G delins
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
Musculoskeletal Diseases 0.010 1.000 1 2018 2018