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.
Bronchogenic Carcinoma
CUI: C0007121
Disease: Bronchogenic Carcinoma
1 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 1991 1991
Rectal Carcinoma
CUI: C0007113
Disease: Rectal Carcinoma
112 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2004 2004
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2006 2006
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
283 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2006 2006
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.030 1.000 3 2002 2008
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.020 1.000 2 2003 2008
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
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
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
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
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
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.030 3 2007 2012
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.030 3 2007 2012
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
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.020 1.000 2 2012 2012
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.020 1.000 2 2012 2012
Acute leukemia
CUI: C0085669
Disease: Acute leukemia
50 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2012 2012
Asthma
CUI: C0004096
Disease: Asthma
1536 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2012 2012