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: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.020 1.000 2 2013 2018
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 0.500 2 2015 2019
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2017 2017
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2017 2017
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.010 1.000 1 2018 2018
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0595989
Disease: Carcinoma of larynx
Carcinoma of larynx
0.010 1.000 1 2015 2015
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.010 1.000 1 2015 2015
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
Squamous cell carcinoma of esophagus
0.010 1.000 1 2018 2018
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
0.010 1.000 1 2019 2019
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0940937
Disease: precancerous lesions
precancerous lesions
0.010 1.000 1 2018 2018
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.010 1.000 1 2016 2016
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0079772
Disease: T-Cell Lymphoma
T-Cell Lymphoma
0.010 1.000 1 2012 2012
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 < 0.001 1 2016 2016
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2019 2019
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0020179
Disease: Huntington Disease
Huntington Disease
0.010 1.000 1 2016 2016
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2019 2019
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0011875
Disease: Diabetic Angiopathies
Diabetic Angiopathies
0.010 1.000 1 2019 2019
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0343641
Disease: Human papilloma virus infection
Human papilloma virus infection
0.010 1.000 1 2018 2018
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0007107
Disease: Malignant neoplasm of larynx
Malignant neoplasm of larynx
0.010 1.000 1 2015 2015
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.010 1.000 1 2016 2016
dbSNP: rs3742330
rs3742330
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2017 2017