rs1048943, CYP1A1

N. diseases: 88
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.020 1.000 2 2007 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.020 1.000 2 2007 2010
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.070 1.000 7 2008 2017
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.060 1.000 6 2008 2017
Uterine Fibroids
CUI: C0042133
Disease: Uterine Fibroids
154 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.040 1.000 4 2008 2016
Head and Neck Carcinoma
CUI: C3887461
Disease: Head and Neck Carcinoma
118 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.020 2 2008 2013
Malignant Head and Neck Neoplasm
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
118 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.020 2 2008 2013
Hereditary Nonpolyposis Colorectal Cancer
CUI: C1333990
Disease: Hereditary Nonpolyposis Colorectal Cancer
1331 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2008 2008
Lynch Syndrome
CUI: C4552100
Disease: Lynch Syndrome
65 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2008 2008
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.030 0.333 3 2009 2014
Bile duct carcinoma
CUI: C0740277
Disease: Bile duct carcinoma
10 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2009 2009
Carcinoma of ampulla of Vater
CUI: C0262401
Disease: Carcinoma of ampulla of Vater
4 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2009 2009
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2009 2009
T-Cell Lymphoma
CUI: C0079772
Disease: T-Cell Lymphoma
24 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2009 2009
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.030 1.000 3 2010 2012
Anxiety
CUI: C0003467
Disease: Anxiety
287 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2010 2010
Hidradenitis Suppurativa
CUI: C0162836
Disease: Hidradenitis Suppurativa
2 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2010 2010
Small cell carcinoma of lung
CUI: C0149925
Disease: Small cell carcinoma of lung
125 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2010 2010
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2010 2010
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.020 1.000 2 2011 2013
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.020 1.000 2 2011 2013
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.020 1.000 2 2011 2013
Fibroid Tumor
CUI: C0023267
Disease: Fibroid Tumor
14 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2011 2011
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.090 1.000 9 2012 2018
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.090 1.000 9 2012 2018