rs587777894, MTOR

N. diseases: 9
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.
FOCAL CORTICAL DYSPLASIA OF TAYLOR
CUI: C1846385
Disease: FOCAL CORTICAL DYSPLASIA OF TAYLOR
27 0.776 0.240 1 11124516 missense variant G/A;T snv 0.800 1.000 4 2015 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.776 0.240 1 11124516 missense variant G/A;T snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.776 0.240 1 11124516 missense variant G/A;T snv 0.700 1.000 1 2016 2016
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.776 0.240 1 11124516 missense variant G/A;T snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.776 0.240 1 11124516 missense variant G/A;T snv 0.700 1.000 1 2016 2016
Papillary renal cell carcinoma, sporadic
CUI: C1336078
Disease: Papillary renal cell carcinoma, sporadic
30 0.776 0.240 1 11124516 missense variant G/A;T snv 0.700 1.000 1 2016 2016
Renal carcinoma
CUI: C1378703
Disease: Renal carcinoma
21 0.776 0.240 1 11124516 missense variant G/A;T snv 0.700 1.000 1 2014 2014
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.776 0.240 1 11124516 missense variant G/A;T snv 0.700 1.000 1 2016 2016
Uterine Cervical Neoplasm
CUI: C0007873
Disease: Uterine Cervical Neoplasm
72 0.776 0.240 1 11124516 missense variant G/A;T snv 0.700 1.000 1 2016 2016