Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs13306035
rs13306035
1.000 0.080 1 186672715 3 prime UTR variant A/G snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2009 2009
dbSNP: rs13306038
rs13306038
1.000 0.080 1 186671995 3 prime UTR variant A/T snv 4.6E-03
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions
0.010 1.000 1 2017 2017
dbSNP: rs201931599
rs201931599
1.000 0.080 1 186671994 3 prime UTR variant T/A snv 1.7E-02
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions
0.010 1.000 1 2017 2017
dbSNP: rs20426
rs20426
1.000 0.080 1 186680288 start lost C/T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2009 2009
dbSNP: rs367650109
rs367650109
1.000 0.080 1 186675959 missense variant A/G snv 4.0E-06 2.1E-05
CUI: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis
0.010 < 0.001 1 2005 2005
dbSNP: rs377655174
rs377655174
1.000 0.080 1 186678374 missense variant G/A snv 8.1E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs4648306
rs4648306
1.000 0.080 1 186671572 downstream gene variant C/T snv 0.12
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions
0.010 1.000 1 2017 2017
dbSNP: rs5276
rs5276
1.000 0.080 1 186673855 3 prime UTR variant C/T snv 4.6E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2009 2009
dbSNP: rs2206593
rs2206593
0.925 0.080 1 186673297 3 prime UTR variant A/G snv 0.95
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 < 0.001 1 2015 2015
dbSNP: rs2206593
rs2206593
0.925 0.080 1 186673297 3 prime UTR variant A/G snv 0.95
CUI: C0030193
Disease: Pain
Pain
0.010 1.000 1 2015 2015
dbSNP: rs2206593
rs2206593
0.925 0.080 1 186673297 3 prime UTR variant A/G snv 0.95
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 < 0.001 1 2015 2015
dbSNP: rs3218625
rs3218625
0.925 0.240 1 186674409 missense variant C/T snv 1.6E-03 5.0E-04
Squamous cell carcinoma of esophagus
0.010 1.000 1 2009 2009
dbSNP: rs3218625
rs3218625
0.925 0.240 1 186674409 missense variant C/T snv 1.6E-03 5.0E-04
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis
0.010 1.000 1 2011 2011
dbSNP: rs373745396
rs373745396
0.925 0.080 1 186679322 missense variant G/A;C;T snv 4.0E-06; 8.0E-06; 4.0E-06
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2013 2013
dbSNP: rs373745396
rs373745396
0.925 0.080 1 186679322 missense variant G/A;C;T snv 4.0E-06; 8.0E-06; 4.0E-06
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs5278
rs5278
0.925 0.080 1 186676537 synonymous variant A/G snv 4.8E-03 1.8E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2009 2009
dbSNP: rs5278
rs5278
0.925 0.080 1 186676537 synonymous variant A/G snv 4.8E-03 1.8E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2009 2009
dbSNP: rs5279
rs5279
0.925 0.080 1 186675946 missense variant A/C;G;T snv 4.0E-06; 4.5E-03; 8.0E-06
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2009 2009
dbSNP: rs5279
rs5279
0.925 0.080 1 186675946 missense variant A/C;G;T snv 4.0E-06; 4.5E-03; 8.0E-06
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2009 2009
dbSNP: rs200479241
rs200479241
0.882 0.080 1 186676073 missense variant T/C snv 2.1E-05
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2012 2012
dbSNP: rs200479241
rs200479241
0.882 0.080 1 186676073 missense variant T/C snv 2.1E-05
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2012 2012
dbSNP: rs200479241
rs200479241
0.882 0.080 1 186676073 missense variant T/C snv 2.1E-05
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2012 2012
dbSNP: rs4648298
rs4648298
0.882 0.120 1 186672550 3 prime UTR variant T/C snv 1.7E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2007 2007
dbSNP: rs4648298
rs4648298
0.882 0.120 1 186672550 3 prime UTR variant T/C snv 1.7E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2009 2009
dbSNP: rs4648298
rs4648298
0.882 0.120 1 186672550 3 prime UTR variant T/C snv 1.7E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2007 2007