rs121913279, PIK3CA

N. diseases: 68
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.
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
362 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.700 15 2004 2012
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
303 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.740 1.000 14 2005 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
226 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.700 13 2004 2016
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
1365 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.780 0.875 12 2004 2015
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
419 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.720 1.000 9 2004 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
1839 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.070 0.857 7 2006 2015
Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi
3 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.800 7 1993 2012
Breast adenocarcinoma
CUI: C0858252
Disease: Breast adenocarcinoma
7 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.700 6 2004 2012
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
240 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.800 6 2004 2012
Epithelial ovarian cancer
CUI: C0677886
Disease: Epithelial ovarian cancer
197 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.800 6 2004 2012
Seborrheic keratosis
CUI: C0022603
Disease: Seborrheic keratosis
12 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.800 6 2004 2012
Stomach Neoplasms
CUI: C0038356
Disease: Stomach Neoplasms
23 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.700 6 2004 2012
Breast Cancer, Familial
CUI: C0346153
Disease: Breast Cancer, Familial
705 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.700 4 2004 2006
Breast Cancer, Familial Male
CUI: C1861906
Disease: Breast Cancer, Familial Male
111 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.700 4 2004 2006
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
159 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.040 1.000 4 2012 2016
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
129 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.020 0.500 2 2014 2016
Rosette-forming glioneuronal tumor of the fourth ventricle
2 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.700 2 2016 2016
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
428 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.700 1 2016 2016
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
121 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.700 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
96 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.700 1 2016 2016
Adrenocortical carcinoma
CUI: C0206686
Disease: Adrenocortical carcinoma
39 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.700 1 2016 2016
Anaplasia
CUI: C0002793
Disease: Anaplasia
4 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.010 1.000 1 2015 2015
Apocrine metaplasia
CUI: C0334036
Disease: Apocrine metaplasia
1 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.010 1.000 1 2013 2013
Ataxia Telangiectasia
CUI: C0004135
Disease: Ataxia Telangiectasia
403 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.010 1.000 1 2015 2015
Biliary Tract Cancer
CUI: C0750952
Disease: Biliary Tract Cancer
10 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.010 1.000 1 2016 2016