rs104886003, PIK3CA

N. diseases: 43
Source: BEFREE ×
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.
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
2154 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.760 1.000 6 2006 2019
Gallbladder Carcinoma
CUI: C0235782
Disease: Gallbladder Carcinoma
65 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.720 1.000 2 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
769 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.720 1.000 2 2008 2019
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
170 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.710 1.000 1 2008 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
78 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.710 1.000 1 2004 2016
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
229 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.710 1.000 1 2005 2016
Uterine Cervical Neoplasm
CUI: C0007873
Disease: Uterine Cervical Neoplasm
4 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.710 1.000 1 2015 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1571 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.100 0.900 10 2009 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2145 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.050 1.000 5 2011 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1441 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.030 1.000 3 2013 2016
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.030 1.000 3 2013 2016
Carcinoma
CUI: C0007097
Disease: Carcinoma
90 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.020 1.000 2 2008 2018
cervical cancer
CUI: C4048328
Disease: cervical cancer
257 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.020 1.000 2 2018 2020
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
266 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.020 1.000 2 2018 2020
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.020 1.000 2 2018 2020
Biliary Tract Cancer
CUI: C0750952
Disease: Biliary Tract Cancer
11 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2015 2015
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
995 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1 2012 2012
Carcinoma, Endometrioid
CUI: C0206687
Disease: Carcinoma, Endometrioid
12 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2020 2020
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
321 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2016 2016
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2012 2012
Cholangiocarcinoma
CUI: C0206698
Disease: Cholangiocarcinoma
41 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2019 2019
Congenital contractural arachnodactyly
CUI: C0220668
Disease: Congenital contractural arachnodactyly
20 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2008 2008
Endometrial Neoplasms
CUI: C0014170
Disease: Endometrial Neoplasms
2 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2020 2020
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
160 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2008 2008
Lymphatic Abnormalities
CUI: C0398368
Disease: Lymphatic Abnormalities
6 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2015 2015