Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1034528
rs1034528
MTOR ; ANGPTL7
0.882 0.120 1 11189075 intron variant G/C snv 0.30
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2016 2016
dbSNP: rs1034528
rs1034528
MTOR ; ANGPTL7
0.882 0.120 1 11189075 intron variant G/C snv 0.30
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2016 2016
dbSNP: rs1034528
rs1034528
MTOR ; ANGPTL7
0.882 0.120 1 11189075 intron variant G/C snv 0.30
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs1034528
rs1034528
MTOR ; ANGPTL7
0.882 0.120 1 11189075 intron variant G/C snv 0.30
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2013 2013
dbSNP: rs1034528
rs1034528
MTOR ; ANGPTL7
0.882 0.120 1 11189075 intron variant G/C snv 0.30
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		0.010 1.000 1 2019 2019
dbSNP: rs1057519777
rs1057519777
MTOR
1.000 0.120 1 11109304 missense variant C/G;T snv
CUI: C1378703
Disease: Renal carcinoma
Renal carcinoma 		0.700 1.000 1 2014 2014
dbSNP: rs1057519778
rs1057519778
MTOR
1.000 0.120 1 11122122 missense variant G/T snv
CUI: C1378703
Disease: Renal carcinoma
Renal carcinoma 		0.700 1.000 1 2014 2014
dbSNP: rs1057519779
rs1057519779
MTOR
0.925 0.200 1 11157242 missense variant A/G snv
CUI: C1378703
Disease: Renal carcinoma
Renal carcinoma 		0.700 1.000 1 2014 2014
dbSNP: rs1057519779
rs1057519779
MTOR
0.925 0.200 1 11157242 missense variant A/G snv
CUI: C1846385
Disease: FOCAL CORTICAL DYSPLASIA OF TAYLOR
FOCAL CORTICAL DYSPLASIA OF TAYLOR 		0.800 0
dbSNP: rs1057519780
rs1057519780
MTOR
1.000 0.120 1 11127800 missense variant C/T snv
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
Transitional cell carcinoma of bladder 		0.700 1.000 1 2014 2014
dbSNP: rs1057519913
rs1057519913
MTOR
0.925 0.120 1 11157172 missense variant G/C snv
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		0.700 1.000 1 2016 2016
dbSNP: rs1057519913
rs1057519913
MTOR
0.925 0.120 1 11157172 missense variant G/C snv
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs1057519913
rs1057519913
MTOR
0.925 0.120 1 11157172 missense variant G/C snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs1057519914
rs1057519914
MTOR
0.851 0.240 1 11157174 missense variant A/G snv
CUI: C1846385
Disease: FOCAL CORTICAL DYSPLASIA OF TAYLOR
FOCAL CORTICAL DYSPLASIA OF TAYLOR 		0.700 1.000 4 2015 2016
dbSNP: rs1057519914
rs1057519914
MTOR
0.851 0.240 1 11157174 missense variant A/G snv
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs1057519914
rs1057519914
MTOR
0.851 0.240 1 11157174 missense variant A/G snv
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		0.700 1.000 1 2016 2016
dbSNP: rs1057519914
rs1057519914
MTOR
0.851 0.240 1 11157174 missense variant A/G snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs1057519914
rs1057519914
MTOR
0.851 0.240 1 11157174 missense variant A/G snv
CUI: C0431391
Disease: Hemimegalencephaly
Hemimegalencephaly 		0.700 0
dbSNP: rs1057519915
rs1057519915
MTOR
0.851 0.160 1 11109318 missense variant A/C snv
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs1057519915
rs1057519915
MTOR
0.851 0.160 1 11109318 missense variant A/C snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs1057519915
rs1057519915
MTOR
0.851 0.160 1 11109318 missense variant A/C snv
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs1057519915
rs1057519915
MTOR
0.851 0.160 1 11109318 missense variant A/C snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs1057519915
rs1057519915
MTOR
0.851 0.160 1 11109318 missense variant A/C snv
CUI: C4225259
Disease: SMITH-KINGSMORE SYNDROME
SMITH-KINGSMORE SYNDROME 		0.700 0
dbSNP: rs1057519916
rs1057519916
MTOR
0.882 0.160 1 11109320 missense variant T/A snv
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs1057519916
rs1057519916
MTOR
0.882 0.160 1 11109320 missense variant T/A snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		0.700 1.000 1 2016 2016