rs867262025, PIK3CA

N. diseases: 10
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.
Overgrowth
CUI: C1849265
Disease: Overgrowth
93 0.790 0.360 3 179221146 missense variant G/A snv 0.700 1.000 14 2006 2018
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.790 0.360 3 179221146 missense variant G/A snv 0.700 1.000 1 2016 2016
Brain Stem Glioma
CUI: C0677865
Disease: Brain Stem Glioma
45 0.790 0.360 3 179221146 missense variant G/A snv 0.700 1.000 1 2016 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.790 0.360 3 179221146 missense variant G/A snv 0.700 1.000 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.790 0.360 3 179221146 missense variant G/A snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
283 0.790 0.360 3 179221146 missense variant G/A snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of the head and neck
348 0.790 0.360 3 179221146 missense variant G/A snv 0.700 1.000 1 2016 2016
Transitional cell carcinoma of bladder
158 0.790 0.360 3 179221146 missense variant G/A snv 0.700 1.000 1 2016 2016
Uterine Cervical Neoplasm
CUI: C0007873
Disease: Uterine Cervical Neoplasm
72 0.790 0.360 3 179221146 missense variant G/A snv 0.700 1.000 1 2016 2016
Megalencephaly cutis marmorata telangiectatica congenita
18 0.790 0.360 3 179221146 missense variant G/A snv 0.700 0