rs1057519941, PIK3CA

N. diseases: 9
Source: CLINVAR ×
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
216 0.776 0.240 3 179203761 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
153 0.776 0.240 3 179203761 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
115 0.776 0.240 3 179203761 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
33 0.776 0.240 3 179203761 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.776 0.240 3 179203761 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
314 0.776 0.240 3 179203761 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of the head and neck
179 0.776 0.240 3 179203761 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Uterine Cervical Neoplasm
CUI: C0007873
Disease: Uterine Cervical Neoplasm
69 0.776 0.240 3 179203761 missense variant T/C;G snv 0.700 1.000 1 2016 2016
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
436 0.776 0.240 3 179203761 missense variant T/C;G snv 0.700 0