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: 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: rs2728127
rs2728127 		0.882 0.120 4 87973963 upstream gene variant A/G;T snv
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: 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: 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: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs2853749
rs2853749 		0.882 0.160 4 87976662 intron variant C/T snv 0.34
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 2 2010 2013
dbSNP: rs2853749
rs2853749 		0.882 0.160 4 87976662 intron variant C/T snv 0.34
CUI: C0018099
Disease: Gout
Gout 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 2 2010 2013
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: 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
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2728127
rs2728127 		0.882 0.120 4 87973963 upstream gene variant A/G;T snv
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: rs2728127
rs2728127 		0.882 0.120 4 87973963 upstream gene variant A/G;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2013 2013
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: 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: 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: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; 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: 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