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: rs1057519849
rs1057519849 		8 127738386 missense variant C/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.700 1.000 1 2014 2014
dbSNP: rs1057519850
rs1057519850 		8 127738447 missense variant C/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.700 1.000 1 2014 2014
dbSNP: rs1057519851
rs1057519851 		8 127738995 missense variant C/G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.700 1.000 1 2014 2014
dbSNP: rs1057519918
rs1057519918 		0.851 0.200 8 127738390 missense variant C/T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs1057519918
rs1057519918 		0.851 0.200 8 127738390 missense variant C/T snv
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1057519918
rs1057519918 		0.851 0.200 8 127738390 missense variant C/T snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs1057519918
rs1057519918 		0.851 0.200 8 127738390 missense variant C/T snv
CUI: C2749484
Disease: NEUROBLASTOMA, SUSCEPTIBILITY TO
NEUROBLASTOMA, SUSCEPTIBILITY TO 		0.700 1.000 1 2016 2016
dbSNP: rs1057519918
rs1057519918 		0.851 0.200 8 127738390 missense variant C/T snv
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs121918683
rs121918683 		1.000 0.160 8 127738519 missense variant A/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.700 1.000 1 2014 2014
dbSNP: rs750664148
rs750664148 		0.851 0.200 8 127738434 missense variant A/C;G snv
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs750664148
rs750664148 		0.851 0.200 8 127738434 missense variant A/C;G snv
CUI: C2749484
Disease: NEUROBLASTOMA, SUSCEPTIBILITY TO
NEUROBLASTOMA, SUSCEPTIBILITY TO 		0.700 1.000 1 2016 2016
dbSNP: rs750664148
rs750664148 		0.851 0.200 8 127738434 missense variant A/C;G snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs750664148
rs750664148 		0.851 0.200 8 127738434 missense variant A/C;G snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs750664148
rs750664148 		0.851 0.200 8 127738434 missense variant A/C;G snv
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs756091827
rs756091827 		0.851 0.200 8 127738435 missense variant C/G;T snv
CUI: C2749484
Disease: NEUROBLASTOMA, SUSCEPTIBILITY TO
NEUROBLASTOMA, SUSCEPTIBILITY TO 		0.700 1.000 1 2016 2016
dbSNP: rs756091827
rs756091827 		0.851 0.200 8 127738435 missense variant C/G;T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs756091827
rs756091827 		0.851 0.200 8 127738435 missense variant C/G;T snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs756091827
rs756091827 		0.851 0.200 8 127738435 missense variant C/G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.700 1.000 1 2014 2014
dbSNP: rs756091827
rs756091827 		0.851 0.200 8 127738435 missense variant C/G;T snv
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs756091827
rs756091827 		0.851 0.200 8 127738435 missense variant C/G;T snv
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs775522201
rs775522201 		8 127738393 missense variant C/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.700 1.000 1 2014 2014
dbSNP: rs121918683
rs121918683 		1.000 0.160 8 127738519 missense variant A/C snv
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma 		Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs121918685
rs121918685 		1.000 0.160 8 127738437 missense variant C/G snv
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma 		Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs28933407
rs28933407 		1.000 0.160 8 127738431 missense variant C/T snv
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma 		Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs117856857
rs117856857 		1.000 0.080 8 127736248 missense variant C/G snv 1.7E-02
CUI: C0016978
Disease: gallbladder neoplasm
gallbladder neoplasm 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015