rs121913274, PIK3CA

N. diseases: 33
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 Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 12 2004 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 10 2004 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.800 1.000 2 2005 2016
melanoma
CUI: C0025202
Disease: melanoma
515 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 2 2014 2014
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 2 2005 2012
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
138 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
108 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Brain Stem Glioma
CUI: C0677865
Disease: Brain Stem Glioma
45 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
COWDEN SYNDROME 5
CUI: C3554518
Disease: COWDEN SYNDROME 5
9 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 1 2013 2013
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Follicular thyroid carcinoma
CUI: C0206682
Disease: Follicular thyroid carcinoma
28 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.010 1.000 1 2011 2011
Gallbladder Carcinoma
CUI: C0235782
Disease: Gallbladder Carcinoma
75 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.010 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Nasopharyngeal Neoplasms
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
36 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
NEVUS, EPIDERMAL (disorder)
CUI: C0334082
Disease: NEVUS, EPIDERMAL (disorder)
17 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.710 1.000 1 2007 2007
Pain
CUI: C0030193
Disease: Pain
196 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.010 1.000 1 2018 2018
Papillary renal cell carcinoma, sporadic
30 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Seborrheic keratosis
CUI: C0022603
Disease: Seborrheic keratosis
21 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.700 1.000 1 2007 2007