Source: BEFREE

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: rs1376199019
rs1376199019
CYP1A1
0.925 0.080 15 74720557 missense variant T/C snv 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.020 1.000 2 2008 2010
dbSNP: rs1279844744
rs1279844744
CYP1A1
0.925 0.080 15 74720521 missense variant A/G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2018 2018
dbSNP: rs1279844744
rs1279844744
CYP1A1
0.925 0.080 15 74720521 missense variant A/G snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.010 1.000 1 2015 2015
dbSNP: rs1279844744
rs1279844744
CYP1A1
0.925 0.080 15 74720521 missense variant A/G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2015 2015
dbSNP: rs1376199019
rs1376199019
CYP1A1
0.925 0.080 15 74720557 missense variant T/C snv 4.0E-06
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2008 2008
dbSNP: rs368952331
rs368952331
CYP1A1
0.925 0.080 15 74722805 missense variant C/T snv 2.8E-05 6.3E-05
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2010 2010
dbSNP: rs368952331
rs368952331
CYP1A1
0.925 0.080 15 74722805 missense variant C/T snv 2.8E-05 6.3E-05
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2010 2010
dbSNP: rs368952331
rs368952331
CYP1A1
0.925 0.080 15 74722805 missense variant C/T snv 2.8E-05 6.3E-05
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 < 0.001 1 2010 2010
dbSNP: rs368952331
rs368952331
CYP1A1
0.925 0.080 15 74722805 missense variant C/T snv 2.8E-05 6.3E-05
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 < 0.001 1 2010 2010
dbSNP: rs4646421
rs4646421
CYP1A1
0.882 0.080 15 74723851 intron variant G/A;C;T snv 0.21
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2016 2016
dbSNP: rs4646421
rs4646421
CYP1A1
0.882 0.080 15 74723851 intron variant G/A;C;T snv 0.21
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2016 2016
dbSNP: rs4646421
rs4646421
CYP1A1
0.882 0.080 15 74723851 intron variant G/A;C;T snv 0.21
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2009 2009
dbSNP: rs56343424
rs56343424
CYP1A1
1.000 0.080 15 74720496 missense variant C/A;T snv 2.1E-03; 3.3E-05
CUI: C0346153
Disease: Breast Cancer, Familial
Breast Cancer, Familial 		0.010 1.000 1 2006 2006
dbSNP: rs766508885
rs766508885
CYP1A1
0.925 0.080 15 74721321 missense variant G/T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2016 2016
dbSNP: rs766508885
rs766508885
CYP1A1
0.925 0.080 15 74721321 missense variant G/T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2016 2016
dbSNP: rs771432878
rs771432878
CYP1A1
0.925 0.080 15 74723013 missense variant A/G snv 4.0E-06 3.5E-05
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.010 1.000 1 2008 2008
dbSNP: rs771432878
rs771432878
CYP1A1
0.925 0.080 15 74723013 missense variant A/G snv 4.0E-06 3.5E-05
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium 		0.010 1.000 1 2008 2008
dbSNP: rs4646422
rs4646422
CYP1A1
0.882 0.120 15 74722964 missense variant C/T snv 1.1E-02 3.4E-03
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids 		0.010 1.000 1 2014 2014
dbSNP: rs4646422
rs4646422
CYP1A1
0.882 0.120 15 74722964 missense variant C/T snv 1.1E-02 3.4E-03
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2014 2014
dbSNP: rs4646422
rs4646422
CYP1A1
0.882 0.120 15 74722964 missense variant C/T snv 1.1E-02 3.4E-03
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 1.000 1 2016 2016
dbSNP: rs4646422
rs4646422
CYP1A1
0.882 0.120 15 74722964 missense variant C/T snv 1.1E-02 3.4E-03
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2016 2016
dbSNP: rs4646422
rs4646422
CYP1A1
0.882 0.120 15 74722964 missense variant C/T snv 1.1E-02 3.4E-03
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2016 2016
dbSNP: rs755133321
rs755133321
CYP1A1
1.000 0.120 15 74723072 missense variant G/A snv 4.1E-06
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.010 1.000 1 2003 2003
dbSNP: rs779682021
rs779682021
CYP1A1
0.882 0.120 15 74721227 missense variant A/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2007 2007
dbSNP: rs779682021
rs779682021
CYP1A1
0.882 0.120 15 74721227 missense variant A/C snv
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids 		0.010 1.000 1 2014 2014