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: rs1989839
rs1989839 		0.790 0.160 3 50341515 intron variant A/G snv 0.22 0.20
CUI: C0153676
Disease: Secondary malignant neoplasm of lung
Secondary malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1989839
rs1989839 		0.790 0.160 3 50341515 intron variant A/G snv 0.22 0.20
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma 		Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs1989839
rs1989839 		0.790 0.160 3 50341515 intron variant A/G snv 0.22 0.20
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs1989839
rs1989839 		0.790 0.160 3 50341515 intron variant A/G snv 0.22 0.20
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: rs1989839
rs1989839 		0.790 0.160 3 50341515 intron variant A/G snv 0.22 0.20
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood Osteosarcoma 		Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs1989839
rs1989839 		0.790 0.160 3 50341515 intron variant A/G snv 0.22 0.20
CUI: C0585442
Disease: Osteosarcoma of bone
Osteosarcoma of bone 		Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs2073498
rs2073498 		0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs2073498
rs2073498 		0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis 		Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2073498
rs2073498 		0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs2073498
rs2073498 		0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs2073498
rs2073498 		0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs2073498
rs2073498 		0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs2073498
rs2073498 		0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		Neoplasms 0.010 1.000 1 2006 2006
dbSNP: rs2236947
rs2236947 		0.882 0.040 3 50334001 intron variant C/A snv 0.39
CUI: C0585442
Disease: Osteosarcoma of bone
Osteosarcoma of bone 		Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs2236947
rs2236947 		0.882 0.040 3 50334001 intron variant C/A snv 0.39
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma 		Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs2236947
rs2236947 		0.882 0.040 3 50334001 intron variant C/A snv 0.39
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood Osteosarcoma 		Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs750917798
rs750917798 		1.000 0.120 3 50331718 missense variant G/A snv 8.0E-06 1.4E-05
CUI: C0085110
Disease: Severe Combined Immunodeficiency
Severe Combined Immunodeficiency 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases 0.010 < 0.001 1 2004 2004
dbSNP: rs898332991
rs898332991 		1.000 0.120 3 50331652 missense variant G/A snv 4.0E-06 4.2E-05
CUI: C0085110
Disease: Severe Combined Immunodeficiency
Severe Combined Immunodeficiency 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases 0.010 < 0.001 1 2004 2004