rs1057519929, 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.
Megalencephaly cutis marmorata telangiectatica congenita
18 0.776 0.320 3 179199066 missense variant G/A snv 0.700 0
Uterine Cervical Neoplasm
CUI: C0007873
Disease: Uterine Cervical Neoplasm
72 0.776 0.320 3 179199066 missense variant G/A snv 0.700 1.000 1 2016 2016
Medulloblastoma
CUI: C0025149
Disease: Medulloblastoma
115 0.776 0.320 3 179199066 missense variant G/A snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.776 0.320 3 179199066 missense variant G/A snv 0.700 1.000 1 2016 2016
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.776 0.320 3 179199066 missense variant G/A snv 0.700 1.000 1 2016 2016
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.776 0.320 3 179199066 missense variant G/A snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of the head and neck
348 0.776 0.320 3 179199066 missense variant G/A snv 0.700 1.000 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.776 0.320 3 179199066 missense variant G/A snv 0.700 1.000 1 2016 2016
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.776 0.320 3 179199066 missense variant G/A snv 0.700 1.000 1 2016 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.776 0.320 3 179199066 missense variant G/A snv 0.700 1.000 1 2016 2016