rs104886003, PIK3CA

N. diseases: 71
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.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.800 1.000 2 2005 2005
Megalencephaly cutis marmorata telangiectatica congenita
CUI: C1865285
Disease: Megalencephaly cutis marmorata telangiectatica congenita
18 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.800 1.000 2 2012 2016
Seborrheic keratosis
CUI: C0022603
Disease: Seborrheic keratosis
21 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.800 1.000 1 2007 2007
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.760 1.000 7 2006 2019
Gallbladder Carcinoma
CUI: C0235782
Disease: Gallbladder Carcinoma
75 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.720 1.000 3 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.720 1.000 3 2008 2019
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.710 1.000 13 2004 2016
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.710 1.000 3 2005 2016
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.710 1.000 2 2008 2016
Uterine Cervical Neoplasm
CUI: C0007873
Disease: Uterine Cervical Neoplasm
72 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.710 1.000 2 2015 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.700 1.000 12 2004 2016
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.700 1.000 11 2004 2012
Head and Neck Neoplasms
CUI: C0018671
Disease: Head and Neck Neoplasms
11 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.700 1.000 2 2013 2014
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.700 1.000 1 2016 2016
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
138 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.700 1.000 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
108 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.700 1.000 1 2016 2016
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.700 1.000 1 2016 2016
Brain Stem Glioma
CUI: C0677865
Disease: Brain Stem Glioma
45 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.700 1.000 1 2016 2016
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.700 1.000 1 2016 2016
Nasopharyngeal Neoplasms
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
36 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.700 1.000 1 2016 2016
Papillary renal cell carcinoma, sporadic
CUI: C1336078
Disease: Papillary renal cell carcinoma, sporadic
30 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.700 1.000 1 2016 2016
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.700 1.000 1 2016 2016