rs121913287, PIK3CA

N. diseases: 12
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 0.752 0.400 3 179199088 missense variant G/A snv 0.700 1.000 3 2009 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.752 0.400 3 179199088 missense variant G/A snv 0.700 1.000 2 2014 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
108 0.752 0.400 3 179199088 missense variant G/A snv 0.700 1.000 1 2016 2016
Brain Stem Glioma
CUI: C0677865
Disease: Brain Stem Glioma
45 0.752 0.400 3 179199088 missense variant G/A snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.752 0.400 3 179199088 missense variant G/A snv 0.700 1.000 1 2016 2016
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.752 0.400 3 179199088 missense variant G/A snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.752 0.400 3 179199088 missense variant G/A snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of the head and neck
348 0.752 0.400 3 179199088 missense variant G/A snv 0.700 1.000 1 2016 2016
Transitional cell carcinoma of bladder
158 0.752 0.400 3 179199088 missense variant G/A snv 0.700 1.000 1 2016 2016
Uterine Carcinosarcoma
CUI: C0280630
Disease: Uterine Carcinosarcoma
80 0.752 0.400 3 179199088 missense variant G/A snv 0.700 1.000 1 2016 2016
Megalencephaly cutis marmorata telangiectatica congenita
18 0.752 0.400 3 179199088 missense variant G/A snv 0.700 0
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.752 0.400 3 179199088 missense variant G/A snv 0.700 0