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: rs11730582
rs11730582 		0.807 0.240 4 87975269 non coding transcript exon variant T/C snv 0.37
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
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: 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: 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: 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: 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: 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: 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: 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: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs28357094
rs28357094 		0.882 0.160 4 87975645 non coding transcript exon variant T/G snv 0.17
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		Cardiovascular Diseases 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: 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: 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: 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: rs2853744
rs2853744 		0.882 0.200 4 87975096 non coding transcript exon variant G/T snv 0.14
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		Nervous System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs2853744
rs2853744 		0.882 0.200 4 87975096 non coding transcript exon variant G/T snv 0.14
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs2853744
rs2853744 		0.882 0.200 4 87975096 non coding transcript exon variant G/T snv 0.14
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs2853749
rs2853749 		0.882 0.160 4 87976662 intron variant C/T snv 0.34
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		Nervous System Diseases 0.010 1.000 1 2016 2016