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
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
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
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
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1000 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1 2012 2012
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
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1 2012 2012
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
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
Squamous cell carcinoma of esophagus
320 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1 2015 2015
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
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
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
246 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2016 2016
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
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
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
197 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2015 2015
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
193 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2017 2017
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
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
169 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2008 2008
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
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
155 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2012 2012
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
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2012 2012
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