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: rs10086908
rs10086908 		1.000 0.080 8 126999692 intron variant T/C snv 0.28
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 2 2015 2019
dbSNP: rs10096351
rs10096351 		1.000 0.080 8 127359926 intron variant A/G snv 0.60
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs1016342
rs1016342 		1.000 0.080 8 127080210 non coding transcript exon variant C/G;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2007 2007
dbSNP: rs1016343
rs1016343 		0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 4 2007 2015
dbSNP: rs1016343
rs1016343 		0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.700 1.000 4 2008 2013
dbSNP: rs1016343
rs1016343 		0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.030 1.000 3 2017 2018
dbSNP: rs1016343
rs1016343 		0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.030 1.000 3 2017 2018
dbSNP: rs1016343
rs1016343 		0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20
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 2019 2019
dbSNP: rs1016343
rs1016343 		0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs1016343
rs1016343 		0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2010 2010
dbSNP: rs1016343
rs1016343 		0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs1026411
rs1026411 		0.827 0.080 8 127014165 intron variant G/A;C snv 0.25
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1026411
rs1026411 		0.827 0.080 8 127014165 intron variant G/A;C snv 0.25
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1026411
rs1026411 		0.827 0.080 8 127014165 intron variant G/A;C snv 0.25
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1026411
rs1026411 		0.827 0.080 8 127014165 intron variant G/A;C snv 0.25
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs1026411
rs1026411 		0.827 0.080 8 127014165 intron variant G/A;C snv 0.25
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1031588
rs1031588 		1.000 0.080 8 127081032 non coding transcript exon variant C/A snv 0.24
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2007 2007
dbSNP: rs10505474
rs10505474 		0.925 0.080 8 127405259 intron variant T/C snv 0.47
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs10505474
rs10505474 		0.925 0.080 8 127405259 intron variant T/C snv 0.47
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs10505474
rs10505474 		0.925 0.080 8 127405259 intron variant T/C snv 0.47
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs10505476
rs10505476 		8 127395871 intron variant C/T snv 0.38
CUI: C0001430
Disease: Adenoma
Adenoma 		Neoplasms 0.010 1.000 1 2008 2008
dbSNP: rs10505476
rs10505476 		8 127395871 intron variant C/T snv 0.38
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2008 2008
dbSNP: rs10505476
rs10505476 		8 127395871 intron variant C/T snv 0.38
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2008 2008
dbSNP: rs10505477
rs10505477 		0.658 0.400 8 127395198 intron variant A/G snv 0.40
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.890 0.938 16 2007 2019
dbSNP: rs10505477
rs10505477 		0.658 0.400 8 127395198 intron variant A/G snv 0.40
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.700 1.000 4 2007 2018